NDC 0781-1684 – Cetirizine Hydrochloride

Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC0781-1684

Product details

Brand name
Cetirizine Hydrochloride
Generic name
Cetirizine Hydrochloride
Labeler
Sandoz Inc
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077946
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
0781-1684-01100 TABLET in 1 BOTTLE (0781-1684-01)Dec 27, 2007
0781-1684-6430 TABLET in 1 BOX, UNIT-DOSE (0781-1684-64)Dec 27, 2007

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