NDC 70710-1684 – Famotidine

Famotidine 40 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70710-1684

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA216441
Marketed since
June 6, 2022
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (5)

Package NDCDescriptionSince
70710-1684-01000 TABLET, FILM COATED in 1 BOTTLE (70710-1684-0)Jun 6, 2022
70710-1684-1100 TABLET, FILM COATED in 1 BOTTLE (70710-1684-1)Jun 6, 2022
70710-1684-330 TABLET, FILM COATED in 1 BOTTLE (70710-1684-3)Jun 6, 2022
70710-1684-410 BLISTER PACK in 1 CARTON (70710-1684-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1684-2)Jun 6, 2022
70710-1684-5500 TABLET, FILM COATED in 1 BOTTLE (70710-1684-5)Jun 6, 2022

Other Famotidine products