NDC 71205-784 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC71205-784

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203769
Marketed since
November 21, 2017
Listing expires
December 31, 2026
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
71205-784-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-784-30)Mar 29, 2023
71205-784-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-784-60)Mar 29, 2023
71205-784-78180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-784-78)Mar 25, 2024
71205-784-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-784-90)Mar 29, 2023

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