METFORMIN HYDROCHLORIDE

Product NDC
71335-9683
11-digit product format
713359683
Labeler code
71335
Product ID
71335-9683_4e6e3035-562a-4663-bf3d-cb2f755702bb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
METFORMIN HYDROCHLORIDE
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA076756
Marketing category
ANDA
Marketing start
2020-08-06
Substance
METFORMIN HYDROCHLORIDE
Active strength
500 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
71335-9683-17133596830160 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9683-1) 2023-04-11NoNoHistorical
71335-9683-27133596830230 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9683-2) 2023-04-11NoNoHistorical
71335-9683-371335968303100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9683-3) 2023-04-11NoNoHistorical
71335-9683-47133596830490 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9683-4) 2023-04-11NoNoHistorical
71335-9683-571335968305120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9683-5) 2023-04-11NoNoHistorical
71335-9683-67133596830615 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9683-6) 2023-04-11NoNoHistorical
71335-9683-77133596830745 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9683-7) 2023-04-11NoNoHistorical
71335-9683-871335968308180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9683-8) 2023-04-11NoNoHistorical
71335-9683-97133596830920 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9683-9) 2023-04-11NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
METFORMIN HYDROCHLORIDEBryant Ranch Prepack2023-04-11HUMAN PRESCRIPTION DRUG LABEL100