Nature Mint Anticavity Fluoride Toothpaste, Sodium monofluorophosphate 0.76%, NET WT 0.85 OZ (24 grams) Tube, Made in India, Dist. by Bob Barker Co. Inc., Fuquay-Varina, NC 27526, NDC 53247-131-03 — Reason: CGMP Deviations — Status: Terminated

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›May 28, 2025recall459d agoAsttraZeneca Pharmaceuticals LP recall (Cls II)AstraZeneca Pharmaceuticals LP

Airsupra (albuterol and budesonide) inhalation aerosol, 90 mcg/80 mcg per inhalation, packaged in a) 120-inhalation canister (NDC 0310-9080-12) b) 28-inhalation canister (NDC 0310-9080-28), Rx only, Manufactured for: AstraZeneca Pharmaceuticals LP, Wilmington, DE 19850, By: AstraZeneca Dunkerque Production (AZDP), Dunkerque, France, Product of France, . — Reason: Defective delivery system — Status: Ongoing

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›May 28, 2025recall459d agoKENIL HEALTHCARE PRIVATE LIMITED recall (Cls II)

Nature Mint Anticavity Fluoride Toothpaste, Sodium monofluorophosphate 0.76%, NET WT 1.5 OZ (43 grams) Tube, Made in India, Dist. by Bob Barker Co. Inc., Fuquay-Varina, NC 27526, NDC 53247-131-04 — Reason: CGMP Deviations — Status: Terminated

full page →fda recalls ↗

›May 28, 2025recall459d agoKENIL HEALTHCARE PRIVATE LIMITED recall (Cls II)

Nature Mint, Anticavity Fluoride Toothpaste, Sodium monofluorophosphate 0.76%, NET WT 2.75 OZ (78g) Tube, Made in India, Dist. by Bob Barker Co. Inc., Fuquay-Varina, NC 27526, NDC 53247-131-05 — Reason: CGMP Deviations — Status: Terminated

full page →fda recalls ↗

›May 28, 2025recall459d agoKENIL HEALTHCARE PRIVATE LIMITED recall (Cls II)

Maximum Security, Anticavity Gel Toothpaste, Sodium Fluoride 0.22%, Fresh Mint Flavor, NET WT 1.5 OZ (43 g) Tube, Made in India, Dist. by Bob Barker Co. Inc., Fuquay-Varina, NC 27526, NDC 53247-132-04 — Reason: CGMP Deviations — Status: Terminated

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›May 28, 2025recall459d agoZydus Pharmaceuticals (USA) Inc recall (Cls II)LB PHARMACEUTICALS INC

Esomeprazole Magnesium for Delayed-Release Oral Suspension, 20 mg, 30-count single dose packets per carton, Rx Only, Manufactured by: Zydus Lifesciences Ltd. Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 68382-848-94 — Reason: Failed Impurities/Degradation Specifications: Out-of-Specification test results obtained for any individual unknown degradation product during Related Compounds testing during long term stability. — Status: Ongoing

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›May 28, 2025recall459d agoKENIL HEALTHCARE PRIVATE LIMITED recall (Cls II)

Maximum Security Anticavity Gel Toothpaste, Sodium Fluoride 0.22%, Fresh Mint Flavor, Net Wt 0.6 OZ (17 g) Tube, Made in India, Dist. by Bob Barker Co. Inc., Fuquay-Varina, NC 27526, NDC 53247-132-02 — Reason: CGMP Deviations — Status: Terminated

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›May 28, 2025recall459d agoKENIL HEALTHCARE PRIVATE LIMITED recall (Cls II)

Optim V, Anti-Itch Cream, Benzocaine 20% & Resorcinol 3% - External analgesic, Net Wt. Peso Neto 1 oz (28g) Tube, Distributed by: Pharmadel LLC, New Castle, DE 19720, Made in India, NDC 55758-300-01, UPC 8 59424 00420 6. — Reason: CGMP Deviations — Status: Terminated

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›May 28, 2025recall459d agoKENIL HEALTHCARE PRIVATE LIMITED recall (Cls II)

Artridon Glucosamine (menthol 2% and Methyl Salicylate 15% - Topical Analgesic), for arthritis joint pain relief, 5 oz (142g) Tube, Dist by/por: Pharmadel LLC, New Castle, DE, 19720, Made in India, NDC 55758-030-05, UPC 8 10096 77151 3. — Reason: CGMP Deviations — Status: Terminated

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›May 28, 2025recall459d agoKENIL HEALTHCARE PRIVATE LIMITED recall (Cls II)Eton Pharmaceuticals, Inc.

Rapidol Maximum Strength, Hydrocortisone 1% Anti-Itch Cream, NET WT 2 oz (60g) Tube, Distributed by: Pharmadel LLC, New Castle, DE, 19720, NDC 55758-420-02, UPC 8 10096 77158 2. — Reason: CGMP Deviations — Status: Terminated

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›May 28, 2025recall459d agoKENIL HEALTHCARE PRIVATE LIMITED recall (Cls II)

Kingskin, SacaCallos, 17% Salicylic acid, 0.5 fl oz (14.8mL) Bottle, Dist. by: Pharmadel LLC, New Castle, DE 19720, Made in India, NDC 55758-423-15, UPC 8 10096 77163 6. — Reason: CGMP Deviations — Status: Terminated

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›May 28, 2025recall459d agoKENIL HEALTHCARE PRIVATE LIMITED recall (Cls II)

Nature Mint, Anticavity Fluoride Toothpaste, Sodium monofluorophosphate 0.76%, NET WT 4.6 OZ (130 grams) Tube, Made in India, Dist. by Bob Barker Co. Inc., Fuquay-Varina, NC 27526, NDC 53247-131-06 — Reason: CGMP Deviations — Status: Terminated

full page →fda recalls ↗

›May 28, 2025recall459d agoKVK Tech, Inc. recall (Cls II)KVK-Tech Inc

Indomethacin Extended-Release Capsules USP, 75 mg, 100-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown, PA, 18940, Made in USA, NDC 10702-016-01. — Reason: cGMP deviations — Status: Ongoing

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›May 28, 2025recall459d agoKENIL HEALTHCARE PRIVATE LIMITED recall (Cls II)

Maximum Security, Anticavity Gel Toothpaste, Sodium Fluoride 0.22%, Fresh Mint Flavor, NET WT 0.85 oz (24 g) Tube, Made in India, Dist. by Bob Barker Co. Inc. Fuquay-Varnia, NC 27526, NDC 53247-132-03 — Reason: CGMP Deviations — Status: Terminated

full page →fda recalls ↗

›May 28, 2025recall459d agoZydus Pharmaceuticals (USA) Inc recall (Cls II)LB PHARMACEUTICALS INC

Esomeprazole Magnesium for Delayed-Release Oral Suspension, 40 mg, 30-count Single-Dose Packets per carton, Rx Only, Manufactured by: Zydus Lifesciences Ltd. Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 68382-849-94 — Reason: Failed Impurities/Degradation Specifications: Out-of-Specification test results obtained for any individual unknown degradation product during Related Compounds testing during long term stability. — Status: Ongoing

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›May 28, 2025recall459d agoKENIL HEALTHCARE PRIVATE LIMITED recall (Cls II)

Maximum Security, Anticavity Gel Toothpaste, Sodium Fluoride 0.22%, Fresh Mint Flavor, NET WT 0.15 OZ (4.25 g) Sachets, Made in India, Dist. by Bob Barker Co. Inc., Fuquay-Varina, NC 27526, NDC 53247-132-01 — Reason: CGMP Deviations — Status: Terminated

full page →fda recalls ↗

›May 28, 2025recall459d agoKENIL HEALTHCARE PRIVATE LIMITED recall (Cls II)

Nature Mint, Anticavity Fluoride Toothpaste, Sodium monofluorophosphate 0.76%, NET WT 0.6 OZ (17g) Tube, Made in India, Dist. by Bob Barker Co. Inc., Fuquay-Varina, NC 27526, NDC 53247-131-02 — Reason: CGMP Deviations — Status: Terminated

full page →fda recalls ↗

›May 28, 2025recall459d agoKENIL HEALTHCARE PRIVATE LIMITED recall (Cls II)

Nature Mint, Anticavity Fluoride Toothpaste, Sodium monofluorophosphate 0.76%, NET WT 6.4 OZ (181 grams) Box, Made in India, Dist. by Bob Barker Co. Inc., Fuquay-Varina, NC 27526, NDC 53247-131-07 — Reason: CGMP Deviations — Status: Terminated

full page →fda recalls ↗

›May 28, 2025recall459d agoKVK Tech, Inc. recall (Cls II)KVK-Tech Inc

Phentermine Hydrochloride Capsules, USP 30mg, 100-count bottle, Rx Only, Mfd. By: KVK-Tech, Inc., Newtown, PA, 18940, Made in USA, NDC 10702-028-01. — Reason: cGMP deviations — Status: Ongoing

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›May 28, 2025recall459d agoKENIL HEALTHCARE PRIVATE LIMITED recall (Cls II)Sun Pharmaceutical Industries Ltd

CURA HONGOS, Antifungal Cream, Clotrimazole 1%, Net Wt/ Peso Neto 2 oz (56.7g) Tube, Distributed by: Pharmadel LLC, New Castle, DE 19720, Made in India, UPC 8 997110 011052. — Reason: CGMP Deviations — Status: Terminated

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›May 28, 2025recall459d agoKENIL HEALTHCARE PRIVATE LIMITED recall (Cls II)

KOFAL Original, Penetrating Pain Relieving Ointment (methyl salicylate 12% - Topical Analgesic), 4 oz (113 g) Jar, Distributed by: Pharmadel LLC, Georgetown, DE 199747, NDC 55758-106-04, UPC 8 9971100128 0. — Reason: CGMP Deviations — Status: Terminated

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›May 28, 2025recall459d agoKENIL HEALTHCARE PRIVATE LIMITED recall (Cls II)Xellia Pharmaceuticals USA LLC

Rapidol, Triple Antibiotic First Aid Ointment, Bacitracin Zinc/ Neomycin Sulfate/ Polymyxin B Sulfate, Net Wt 2 oz (56g) Tube, Distributed by: Pharmadel LLC, New Castle, DE, 19720, Made in India, NDC 55758-440-02, UPC 8 10096 77162 9. — Reason: CGMP Deviations — Status: Terminated

full page →fda recalls ↗

›May 28, 2025recall459d agoKENIL HEALTHCARE PRIVATE LIMITED recall (Cls II)

KOFAL, Athletes, Penetrating Pain Relief, External Analgesic Ointment (methyl salicylate 10.5% - External Analgesic), 2 oz (60 g) Jar, Distributed by: Pharmadel LLC, New Castle, DE 19720, NDC 55758-109-02, UPC 8 99711 00101 3. — Reason: CGMP Deviations — Status: Terminated

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›May 28, 2025recall459d agoKENIL HEALTHCARE PRIVATE LIMITED recall (Cls II)Bharati Vidyapeeth Deemed University

Cinnafresh anticavity gel toothpaste, sodium fluoride 0.22%, Bold Cinnamon Flavor, NET WT. 0.85 OZ (24 grams) Tube, Made in India, Dist. by Bob Barker Co. Inc., Fuquay-Varina, NC 27526, NDC 53247-133-01 — Reason: CGMP Deviations — Status: Terminated

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›May 28, 2025recall459d agoCareFusion 213, LLC recall (Cls II)Coorg Instituite of Dental Sciences

BD ChloraPrep Clear, 2% x/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA), Patient Preoperative Skin Preparation, Sterile Solution, Applicator is sterile if package is intact, Flammable, External Use Only, 1 mL Applicator per pouch, 60 Applicators per inner carton, CareFusion 213, LLC, El Paso, TX 79912, subsidiary of Becton, Dickinson and Co., Made in the USA, Catalog Number 930480, NDC 54365-400-31. — Reason: Lack of Assurance of Sterility: The affected product may exhibit an open seal on the packaging of the applicator. — Status: Ongoing

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›May 28, 2025recall459d agoKENIL HEALTHCARE PRIVATE LIMITED recall (Cls II)Sun Pharmaceutical Industries Ltd

CURA HONGOS, Antifungal, 1% Clotrimazole, Topical Lotion, 0.76 fl oz (22.5 mL) Bottle, Dist by/por: Pharmadel LLC, New Castle, DE 19720, Made in India, NDC 55758-34-01, UPC 8 10096 77170 4. — Reason: CGMP Deviations — Status: Terminated

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›May 29, 2025approval458d agoFOCINVEZ (FOSAPREPITANT DIMEGLUMINE) — FDA approvalAthenex Inc (Inactive)

Sponsor: STERISCIENCE. Form: SOLUTION. Route: INTRAVENOUS

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›May 29, 2025approval458d agoMETHOTREXATE — FDA approvalMaxtrex

Sponsor: ACCORD HLTHCARE. Form: SOLUTION. Route: INTRAVENOUS

full page →Maxtrex →fda approvals ↗

›May 30, 2025approval457d agoACETAZOLAMIDE — FDA approvalACETAZOLAMIDE

Sponsor: AUROBINDO PHARMA LTD. Form: TABLET. Route: ORAL

full page →ACETAZOLAMIDE →fda approvals ↗

453d ago

ISOTRETINOIN — FDA approvalSun Pharmaceutical Industries Ltd

Sponsor: ACTAVIS LABS FL. Form: CAPSULE. Route: ORAL

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›Jun 3, 2025approval453d agoMYORISAN (ISOTRETINOIN) — FDA approvalSun Pharmaceutical Industries Ltd

Sponsor: UPSHER SMITH LABS. Form: CAPSULE. Route: ORAL

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›Jun 4, 2025recall452d agoGlenmark Pharmaceuticals Inc., USA recall (Cls II)LB PHARMACEUTICALS INC

Carvedilol Tablets USP 25 mg, 500 -Count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured for Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430. NDC 68462-165-05. — Reason: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit — Status: Ongoing

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›Jun 4, 2025recall452d agoGlenmark Pharmaceuticals Inc., USA recall (Cls II)LB PHARMACEUTICALS INC

Carvedilol Tablets USP 12.5 mg, 500-Count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured for Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430. NDC: 68462-164-05 — Reason: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit — Status: Ongoing

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›Jun 4, 2025recall452d agoGlenmark Pharmaceuticals Inc., USA recall (Cls II)LB PHARMACEUTICALS INC

Theophylline (Anhydrous) Extended-Release Tablets, 600 mg, 100 Tablets per bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited. Colvale-Bardez, Goa - 403513, India. Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430. NDC: 68462-356-01 — Reason: OOS results reported for the Dissolution (by UV) test. — Status: Ongoing

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$BMY66.58-0.55%

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$LBRX47.73-0.33%

$NVO45.61-1.41%

$LBRX47.73-0.33%

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