Package 0904-7510-61

Brand: cetirizine

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7510-61
Digits Only 0904751061
Product NDC 0904-7510
Description

100 BLISTER PACK in 1 CARTON (0904-7510-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-04-07
Brand cetirizine
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d354746c-e39d-41b4-b864-db8f4db73a03", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["71db132d-dca4-47ef-8560-c68ad2258933"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7510-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7510-61", "marketing_start_date": "20250407"}], "brand_name": "Cetirizine", "product_id": "0904-7510_d354746c-e39d-41b4-b864-db8f4db73a03", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0904-7510", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078336", "marketing_category": "ANDA", "marketing_start_date": "20250407", "listing_expiration_date": "20271231"}