NDC 46708-293 – Famotidine

Famotidine 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC46708-293

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078916
Marketed since
January 29, 2016
Listing expires
December 31, 2027
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (5)

Package NDCDescriptionSince
46708-293-10100 TABLET in 1 CARTON (46708-293-10)Jan 29, 2016
46708-293-3030 TABLET in 1 BOTTLE (46708-293-30)Jan 29, 2016
46708-293-31100 TABLET in 1 BOTTLE (46708-293-31)Jan 29, 2016
46708-293-71500 TABLET in 1 BOTTLE (46708-293-71)Jan 29, 2016
46708-293-911000 TABLET in 1 BOTTLE (46708-293-91)Jan 29, 2016

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