Metformin Hydrochloride

Product NDC
50090-7278
11-digit product format
500907278
Labeler code
50090
Product ID
50090-7278_93150ddc-f497-4290-af58-6d1d9deafe4c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metformin Hydrochloride
Dosage form
TABLET, COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA205096
Marketing category
ANDA
Marketing start
2024-03-04
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
50090-7278-05009072780060 TABLET, COATED in 1 BOTTLE (50090-7278-0) 2024-10-08NoNoHistorical
50090-7278-350090727803100 TABLET, COATED in 1 BOTTLE (50090-7278-3) 2024-10-08NoNoHistorical
50090-7278-45009072780430 TABLET, COATED in 1 BOTTLE (50090-7278-4) 2024-10-08NoNoHistorical
50090-7278-550090727805180 TABLET, COATED in 1 BOTTLE (50090-7278-5) 2024-10-08NoNoHistorical
50090-7278-65009072780690 TABLET, COATED in 1 BOTTLE (50090-7278-6) 2024-10-08NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Metformin HydrochlorideA-S Medication Solutions2024-10-14HUMAN PRESCRIPTION DRUG LABEL1