NDC 71205-884 – Metformin Hydrochloride

Metformin Hydrochloride 1000 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71205-884

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 (9)

Package NDCDescriptionSince
71205-884-00100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-884-00)Nov 8, 2021
71205-884-111000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-884-11)Nov 8, 2021
71205-884-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-884-30)Nov 8, 2021
71205-884-55500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-884-55)Nov 8, 2021
71205-884-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-884-60)Nov 8, 2021
71205-884-64240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-884-64)Nov 8, 2021
71205-884-72120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-884-72)Nov 8, 2021
71205-884-78180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-884-78)Nov 8, 2021
71205-884-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-884-90)Nov 8, 2021

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