Metformin HCl

Product NDC
72789-189
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metformin HCl
Dosage form
TABLET
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA090564
Marketing category
ANDA
Substance
METFORMIN HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72789-189-2121 TABLET in 1 BOTTLE, PLASTIC (72789-189-21) 2021-06-15NoHistorical
72789-189-3030 TABLET in 1 BOTTLE, PLASTIC (72789-189-30) 2021-05-10NoHistorical
72789-189-4242 TABLET in 1 BOTTLE, PLASTIC (72789-189-42) 2025-11-04NoHistorical
72789-189-6060 TABLET in 1 BOTTLE, PLASTIC (72789-189-60) 2021-05-25NoHistorical
72789-189-9090 TABLET in 1 BOTTLE, PLASTIC (72789-189-90) 2021-05-18NoHistorical
72789-189-93180 TABLET in 1 BOTTLE, PLASTIC (72789-189-93) 2021-05-10NoHistorical
72789-189-98120 TABLET in 1 BOTTLE, PLASTIC (72789-189-98) 2021-10-28NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Metformin Hydrochloride Tablets USPPD-Rx Pharmaceuticals, Inc.2025-11-04HUMAN PRESCRIPTION DRUG LABEL14
Metformin Hydrochloride Tablets USPPD-Rx Pharmaceuticals, Inc.2024-07-12HUMAN PRESCRIPTION DRUG LABEL12