NDC 0615-8558 – Famotidine

Famotidine 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0615-8558

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
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 (3)

Package NDCDescriptionSince
0615-8558-0515 TABLET in 1 BLISTER PACK (0615-8558-05)Jan 16, 2025
0615-8558-2828 TABLET in 1 BLISTER PACK (0615-8558-28)Jan 16, 2025
0615-8558-3930 TABLET in 1 BLISTER PACK (0615-8558-39)Jan 16, 2025

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