NDC 0093-8204 – Cimetidine

Cimetidine 400 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0093-8204

Product details

Brand name
Cimetidine
Generic name
Cimetidine
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA074151
Marketed since
February 2, 2004
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Cimetidine →

Package NDC codes (2)

Package NDCDescriptionSince
0093-8204-01100 TABLET, FILM COATED in 1 BOTTLE (0093-8204-01)Apr 7, 2004
0093-8204-05500 TABLET, FILM COATED in 1 BOTTLE (0093-8204-05)Feb 2, 2004

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