Package 16571-401-10

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 16571-401-10
Digits Only 1657140110
Product NDC 16571-401
Product ID 16571-401_37fb3dd8-d5bf-46e4-8331-0c8c1eac540d
Description

100 TABLET in 1 BOTTLE (16571-401-10)

Marketing

Marketing Status
Marketed Since 2009-10-01
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": "37fb3dd8-d5bf-46e4-8331-0c8c1eac540d", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014676"], "spl_set_id": ["6493d4f6-dead-45ec-ade1-28ce624af33d"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16571-401-10)", "package_ndc": "16571-401-10", "marketing_start_date": "20091001"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "16571-401_37fb3dd8-d5bf-46e4-8331-0c8c1eac540d", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "16571-401", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA077829", "marketing_category": "ANDA", "marketing_start_date": "20091001", "listing_expiration_date": "20261231"}