Metformin Hydrochloride

Product NDC
71335-2533
11-digit product format
713352533
Labeler code
71335
Product ID
71335-2533_e56912bc-7e1f-4c23-a23e-2c0e094c6b2c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metformin Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA209882
Marketing category
ANDA
Marketing start
2021-05-17
Substance
METFORMIN HYDROCHLORIDE
Active strength
1000 mg/1
Pharmacologic classes
Biguanide [EPC], Biguanides [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
786Z46389EMETFORMIN HYDROCHLORIDE1115-70-4METFORMIN HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71335-2533-0713352533001000 TABLET, FILM COATED in 1 BOTTLE (71335-2533-0) 2024-12-10NoNoHistorical
71335-2533-17133525330160 TABLET, FILM COATED in 1 BOTTLE (71335-2533-1) 2024-12-10NoNoHistorical
71335-2533-271335253302100 TABLET, FILM COATED in 1 BOTTLE (71335-2533-2) 2024-12-10NoNoHistorical
71335-2533-37133525330330 TABLET, FILM COATED in 1 BOTTLE (71335-2533-3) 2024-12-10NoNoHistorical
71335-2533-471335253304120 TABLET, FILM COATED in 1 BOTTLE (71335-2533-4) 2024-12-10NoNoHistorical
71335-2533-57133525330590 TABLET, FILM COATED in 1 BOTTLE (71335-2533-5) 2024-12-10NoNoHistorical
71335-2533-67133525330628 TABLET, FILM COATED in 1 BOTTLE (71335-2533-6) 2024-12-10NoNoHistorical
71335-2533-77133525330756 TABLET, FILM COATED in 1 BOTTLE (71335-2533-7) 2024-12-10NoNoHistorical
71335-2533-871335253308180 TABLET, FILM COATED in 1 BOTTLE (71335-2533-8) 2024-12-10NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Metformin HydrochlorideBryant Ranch Prepack2024-12-10HUMAN PRESCRIPTION DRUG LABEL1