NDC 72205-145 – Famotidine

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

Human Prescription Drug

Product NDC72205-145

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Novadoz Pharmaceuticals LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA217400
Marketed since
August 6, 2024
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (6)

Package NDCDescriptionSince
72205-145-05500 TABLET, FILM COATED in 1 BOTTLE (72205-145-05)Sep 18, 2024
72205-145-3030 TABLET, FILM COATED in 1 BOTTLE (72205-145-30)Sep 18, 2024
72205-145-5050 TABLET, FILM COATED in 1 BOTTLE (72205-145-50)Nov 12, 2025
72205-145-91100 TABLET, FILM COATED in 1 BOTTLE (72205-145-91)Sep 18, 2024
72205-145-9875 TABLET, FILM COATED in 1 BOTTLE (72205-145-98)Nov 12, 2025
72205-145-991000 TABLET, FILM COATED in 1 BOTTLE (72205-145-99)Sep 18, 2024

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