NDC 68788-8756 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC68788-8756

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209882
Marketed since
October 14, 2024
Listing expires
December 31, 2027
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
68788-8756-1100 TABLET, FILM COATED in 1 BOTTLE (68788-8756-1)Oct 14, 2024
68788-8756-330 TABLET, FILM COATED in 1 BOTTLE (68788-8756-3)Oct 14, 2024
68788-8756-660 TABLET, FILM COATED in 1 BOTTLE (68788-8756-6)Oct 14, 2024
68788-8756-8120 TABLET, FILM COATED in 1 BOTTLE (68788-8756-8)Oct 14, 2024
68788-8756-990 TABLET, FILM COATED in 1 BOTTLE (68788-8756-9)Oct 14, 2024

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