Metformin Hydrochloride

Product NDC
50090-6753
11-digit product format
500906753
Labeler code
50090
Product ID
50090-6753_d0143d34-a44c-46ae-abe5-04e8bdeaf6a3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metformin Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA090564
Marketing category
ANDA
Marketing start
2019-06-26
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
50090-6753-05009067530060 TABLET in 1 BOTTLE (50090-6753-0) 60 tablet2023-10-19NoNoHistorical
50090-6753-250090675302100 TABLET in 1 BOTTLE (50090-6753-2) 100 tablet2023-10-17NoNoHistorical
50090-6753-45009067530490 TABLET in 1 BOTTLE (50090-6753-4) 90 tablet2023-10-17NoNoHistorical
50090-6753-550090675305180 TABLET in 1 BOTTLE (50090-6753-5) 180 tablet2023-10-17NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Metformin HydrochlorideA-S Medication Solutions2023-10-20HUMAN PRESCRIPTION DRUG LABEL3