Package 68071-2571-7

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-2571-7
Digits Only 6807125717
Product NDC 68071-2571
Product ID 68071-2571_fd90ffc6-a1de-e02e-e053-6294a90a4e7c
Description

7 TABLET in 1 BOTTLE (68071-2571-7)

Marketing

Marketing Status
Marketed Since 2021-11-15
Brand cetirizine hydrochloride
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Cetirizine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fd90ffc6-a1de-e02e-e053-6294a90a4e7c", "openfda": {"upc": ["0368071257175"], "unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["d0d8b376-9001-8776-e053-2a95a90ae651"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET in 1 BOTTLE (68071-2571-7)", "package_ndc": "68071-2571-7", "marketing_start_date": "20211115"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "68071-2571_fd90ffc6-a1de-e02e-e053-6294a90a4e7c", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68071-2571", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077498", "marketing_category": "ANDA", "marketing_start_date": "20071227", "listing_expiration_date": "20261231"}