NDC 68788-8498 – Metformin Hydrochloride

Metformin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68788-8498

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
August 1, 2023
Listing expires
December 31, 2026
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
68788-8498-1100 TABLET, FILM COATED in 1 BOTTLE (68788-8498-1)Aug 1, 2023
68788-8498-330 TABLET, FILM COATED in 1 BOTTLE (68788-8498-3)Aug 1, 2023
68788-8498-660 TABLET, FILM COATED in 1 BOTTLE (68788-8498-6)Aug 1, 2023
68788-8498-7180 TABLET, FILM COATED in 1 BOTTLE (68788-8498-7)Aug 1, 2023
68788-8498-8120 TABLET, FILM COATED in 1 BOTTLE (68788-8498-8)Aug 1, 2023
68788-8498-990 TABLET, FILM COATED in 1 BOTTLE (68788-8498-9)Aug 1, 2023

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