NDC 82804-194 – Famotidine

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

Human Prescription Drug

Product NDC82804-194

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075718
Marketed since
April 16, 2001
Listing expires
December 31, 2027
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (6)

Package NDCDescriptionSince
82804-194-066 TABLET, FILM COATED in 1 BOTTLE (82804-194-06)Jun 1, 2026
82804-194-1010 TABLET, FILM COATED in 1 BOTTLE (82804-194-10)May 28, 2025
82804-194-3030 TABLET, FILM COATED in 1 BOTTLE (82804-194-30)Apr 25, 2025
82804-194-6060 TABLET, FILM COATED in 1 BOTTLE (82804-194-60)Apr 23, 2026
82804-194-78180 TABLET, FILM COATED in 1 BOTTLE (82804-194-78)Jun 5, 2025
82804-194-9090 TABLET, FILM COATED in 1 BOTTLE (82804-194-90)Feb 4, 2025

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