NDC 59651-855 – Metformin Hydrochloride

Metformin Hydrochloride 850 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC59651-855

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077095
Marketed since
March 29, 2024
Listing expires
December 31, 2027
Pharmacologic class
Biguanide

Active ingredients

Uses, dosage, side effects and warnings for Metformin hydrochloride →

Package NDC codes (8)

Package NDCDescriptionSince
59651-855-01100 TABLET, FILM COATED in 1 BOTTLE (59651-855-01)Mar 29, 2024
59651-855-05500 TABLET, FILM COATED in 1 BOTTLE (59651-855-05)Mar 29, 2024
59651-855-262500 TABLET, FILM COATED in 1 BOTTLE (59651-855-26)Mar 29, 2024
59651-855-5050 TABLET, FILM COATED in 1 BOTTLE (59651-855-50)Mar 29, 2024
59651-855-6060 TABLET, FILM COATED in 1 BOTTLE (59651-855-60)Mar 29, 2024
59651-855-79300 TABLET, FILM COATED in 1 BOTTLE (59651-855-79)Mar 29, 2024
59651-855-9090 TABLET, FILM COATED in 1 BOTTLE (59651-855-90)Mar 29, 2024
59651-855-991000 TABLET, FILM COATED in 1 BOTTLE (59651-855-99)Mar 29, 2024

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