NDC 63187-723 – Famotidine

Famotidine 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63187-723

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078916
Marketed since
January 29, 2016
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
63187-723-00100 TABLET in 1 BOTTLE (63187-723-00)Jun 1, 2016
63187-723-066 TABLET in 1 BOTTLE (63187-723-06)Sep 1, 2019
63187-723-1010 TABLET in 1 BOTTLE (63187-723-10)Nov 1, 2016
63187-723-3030 TABLET in 1 BOTTLE (63187-723-30)Jun 1, 2016
63187-723-6060 TABLET in 1 BOTTLE (63187-723-60)Jun 1, 2016
63187-723-9090 TABLET in 1 BOTTLE (63187-723-90)Jun 1, 2016

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