NDC 43063-695 – Famotidine

Famotidine 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC43063-695

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075805
Marketed since
April 16, 2001
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
43063-695-2020 TABLET in 1 BOTTLE, PLASTIC (43063-695-20)Feb 21, 2017
43063-695-3030 TABLET in 1 BOTTLE, PLASTIC (43063-695-30)Jul 26, 2016
43063-695-6060 TABLET in 1 BOTTLE, PLASTIC (43063-695-60)Jul 26, 2016
43063-695-9090 TABLET in 1 BOTTLE, PLASTIC (43063-695-90)Jul 26, 2016
43063-695-93180 TABLET in 1 BOTTLE, PLASTIC (43063-695-93)Jul 26, 2016
43063-695-951000 TABLET in 1 BOTTLE, PLASTIC (43063-695-95)Feb 22, 2021

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