NDC 25000-087 – Famotidine 20 mg

Famotidine 20 mg/1 · Tablet, Coated · Oral

Human Otc Drug

Product NDC25000-087

Product details

Brand name
Famotidine 20 mg
Generic name
Famotidine 20 mg
Labeler
MARKSANS PHARMA LIMITED
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA217543
Marketed since
March 10, 2023
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine 20 mg →

Package NDC codes (5)

Package NDCDescriptionSince
25000-087-031 BOTTLE in 1 CARTON (25000-087-03) / 30 TABLET, COATED in 1 BOTTLEMar 10, 2023
25000-087-051 BOTTLE in 1 CARTON (25000-087-05) / 50 TABLET, COATED in 1 BOTTLEApr 24, 2024
25000-087-081 BOTTLE in 1 CARTON (25000-087-08) / 100 TABLET, COATED in 1 BOTTLEMar 10, 2023
25000-087-363 BLISTER PACK in 1 CARTON (25000-087-36) / 10 TABLET, COATED in 1 BLISTER PACKMar 10, 2023
25000-087-821 BOTTLE in 1 CARTON (25000-087-82) / 200 TABLET, COATED in 1 BOTTLEFeb 15, 2024

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