NDC 71205-882 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC71205-882

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
71205-882-00100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-882-00)Nov 8, 2021
71205-882-111000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-882-11)Nov 8, 2021
71205-882-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-882-30)Nov 8, 2021
71205-882-55500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-882-55)Nov 8, 2021
71205-882-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-882-60)Nov 8, 2021
71205-882-64240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-882-64)Nov 8, 2021
71205-882-72120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-882-72)Nov 8, 2021
71205-882-78180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-882-78)Nov 8, 2021
71205-882-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-882-90)Nov 8, 2021

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