fda
11 records
FDA Drug Recall: Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufacture
2025-01-22
Class III — Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
View Source
FDA Drug Recall: Diphenhydramine HCl 25 mg, 1000 Capsules per bottle, Akron Pharma, Manufactured
2025-01-22
Class III — Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
View Source
FDA Drug Recall: Diphenhydramine HCl 50 mg, 1000 capsules per bottle, Akron Pharma, Manufactured
2025-01-22
Class III — Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
View Source
FDA Drug Recall: Acetaminophen Regular Strength, 325 mg, 100 Tablets per bottle, Akron Pharma, In
2025-01-22
Class III — Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
View Source
FDA Drug Recall: Diphenhydramine HCl 25 mg, 100 capsules per bottle, Akron Pharma, Manufactured f
2025-01-22
Class III — Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
View Source
FDA Drug Recall: Acetaminophen Extra Strength 500 mg, 100 Tablets per bottle, Akron Pharma, Inc.,
2025-01-22
Class III — Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
View Source
FDA Drug Recall: Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma, Manu
2025-01-22
Class III — Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
View Source
FDA Drug Recall: OneLAX Docusate Sodium Liquid (docusate sodium 50 mg/5 mL) Stool Softener Laxati
2024-10-30
Class II — CGMP Deviations
View Source
FDA Drug Recall: DIBUCAINE 1% HEMORRHOIDAL OINTMENT, 1 oz. (28 gm), Manufactured for: Akron Pharm
2023-03-15
Class III — Labeling: Incorrect or Missing Lot and/or Exp Date
View Source
FDA Drug Recall: Acetaminophen 500 mg tablet, Extra Strength, packaged in a) 100-count bottle (ND
2022-08-24
Class III — Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
View Source
FDA Drug Recall: Acetaminophen 325 mg tablets, packaged in a) 100-count bottle (NDC 71399-8024-0
2022-08-24
Class III — Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
View Source
fda_adverse
3 records
FDA AE Manufacturer: AKRON PHARMA INC
Drug adverse event reporter — Product: CALCIUM CARBONATE
View Source
FDA AE Manufacturer: Akron Pharma Inc.
Drug adverse event reporter — Product: ACETAMINOPHEN
View Source
ny_corps
1 records
NY Corp: AKRON PHARMA INC.
2022-12-01
FOREIGN BUSINESS CORPORATION | County: Suffolk | Jurisdiction: New Jersey
View Source
Be informed when major changes happen on C.F.A.I. — new data sources, platform updates, critical enforcement alerts
No spam. Only major updates. Unsubscribe anytime.