NDC 0378-3637 – Cetirizine Hydrochloride

Cetirizine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral

Human Otc Drug

Product NDC0378-3637

Product details

Brand name
Cetirizine Hydrochloride
Generic name
Cetirizine hydrochloride
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076677
Marketed since
December 27, 2007
Listing expires
December 31, 2026
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Cetirizine hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
0378-3637-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3637-01)Dec 27, 2007
0378-3637-05500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3637-05)Dec 27, 2007

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