NDC 42385-948 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC42385-948

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Laurus Labs Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209882
Marketed since
May 17, 2021
Listing expires
December 31, 2027
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
42385-948-01100 TABLET, FILM COATED in 1 BOTTLE (42385-948-01)Jul 20, 2021
42385-948-05500 TABLET, FILM COATED in 1 BOTTLE (42385-948-05)Jul 20, 2021
42385-948-111000 TABLET, FILM COATED in 1 BOTTLE (42385-948-11)May 17, 2021
42385-948-18180 TABLET, FILM COATED in 1 BOTTLE (42385-948-18)Jul 20, 2021
42385-948-1910 BLISTER PACK in 1 CARTON (42385-948-19) / 10 TABLET, FILM COATED in 1 BLISTER PACKMay 17, 2021
42385-948-9090 TABLET, FILM COATED in 1 BOTTLE (42385-948-90)May 17, 2021

Other Metformin hydrochloride products