NDC 0904-6717 – Cetirizine

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

Human Otc Drug

Product NDC0904-6717

Product details

Brand name
Cetirizine
Generic name
Cetirizine Hydrochloride
Labeler
Major Pharmaceuticals
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078336
Marketed since
June 29, 2018
Listing expires
December 31, 2027
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Cetirizine →

Package NDC codes (7)

Package NDCDescriptionSince
0904-6717-40500 TABLET, FILM COATED in 1 BOTTLE (0904-6717-40)Jul 3, 2018
0904-6717-4114 BLISTER PACK in 1 CARTON (0904-6717-41) / 1 TABLET, FILM COATED in 1 BLISTER PACKJun 29, 2018
0904-6717-431 BOTTLE in 1 CARTON (0904-6717-43) / 45 TABLET, FILM COATED in 1 BOTTLEJul 3, 2018
0904-6717-461 BOTTLE in 1 CARTON (0904-6717-46) / 30 TABLET, FILM COATED in 1 BOTTLEJul 3, 2018
0904-6717-601 BOTTLE in 1 CARTON (0904-6717-60) / 100 TABLET, FILM COATED in 1 BOTTLEJul 3, 2018
0904-6717-721 BOTTLE in 1 CARTON (0904-6717-72) / 300 TABLET, FILM COATED in 1 BOTTLEJul 3, 2018
0904-6717-861 BOTTLE in 1 CARTON (0904-6717-86) / 90 TABLET, FILM COATED in 1 BOTTLEJul 3, 2018

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