NDC 72865-214 – Famotidine

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

Human Prescription Drug

Product NDC72865-214

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
XLCare Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215689
Marketed since
October 15, 2021
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (4)

Package NDCDescriptionSince
72865-214-01100 TABLET, FILM COATED in 1 BOTTLE (72865-214-01)Oct 15, 2021
72865-214-05500 TABLET, FILM COATED in 1 BOTTLE (72865-214-05)Oct 15, 2021
72865-214-18180 TABLET, FILM COATED in 1 BOTTLE (72865-214-18)Oct 15, 2021
72865-214-3030 TABLET, FILM COATED in 1 BOTTLE (72865-214-30)Oct 15, 2021

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