NDC 70518-3829 – Famotidine

Famotidine 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70518-3829

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215630
Marketed since
August 15, 2023
Listing expires
December 31, 2027
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (8)

Package NDCDescriptionSince
70518-3829-130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-1)Nov 6, 2023
70518-3829-390 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-3)Jan 24, 2024
70518-3829-490 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-4)Feb 28, 2024
70518-3829-530 TABLET, FILM COATED in 1 BLISTER PACK (70518-3829-5)Jun 12, 2024
70518-3829-614 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-6)Nov 21, 2024
70518-3829-760 TABLET, FILM COATED in 1 BLISTER PACK (70518-3829-7)Jan 4, 2025
70518-3829-814 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-8)Jan 14, 2025
70518-3829-925 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-9)Oct 15, 2025

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