METFORMIN HYDROCHLORIDE

Product NDC
71335-1785
11-digit product format
713351785
Labeler code
71335
Product ID
71335-1785_254bf7ea-fed6-4ed5-a868-9c64ce3b8fd5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
METFORMIN HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA203769
Marketing category
ANDA
Marketing start
2018-01-15
Substance
METFORMIN HYDROCHLORIDE
Active strength
850 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 formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-1785-17133517850160 TABLET in 1 BOTTLE, PLASTIC (71335-1785-1) 60 tablet2021-03-10NoNoHistorical
71335-1785-27133517850230 TABLET in 1 BOTTLE, PLASTIC (71335-1785-2) 30 tablet2021-03-10NoNoHistorical
71335-1785-371335178503120 TABLET in 1 BOTTLE, PLASTIC (71335-1785-3) 120 tablet2021-03-10NoNoHistorical
71335-1785-47133517850490 TABLET in 1 BOTTLE, PLASTIC (71335-1785-4) 90 tablet2021-03-10NoNoHistorical
71335-1785-571335178505100 TABLET in 1 BOTTLE, PLASTIC (71335-1785-5) 100 tablet2021-03-10NoNoHistorical
71335-1785-671335178506180 TABLET in 1 BOTTLE, PLASTIC (71335-1785-6) 180 tablet2021-03-10NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
METFORMIN HYDROCHLORIDEBryant Ranch Prepack2021-03-10HUMAN PRESCRIPTION DRUG LABEL100