Package 16571-402-10

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 16571-402-10
Digits Only 1657140210
Product NDC 16571-402
Description

100 TABLET in 1 BOTTLE (16571-402-10)

Marketing

Marketing Status
Marketed Since 2009-10-01
Brand cetirizine hydrochloride
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "76ebe5e7-afda-45c3-bf06-07e37827a07a", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["5481ccb3-b311-4b25-b923-4fe8522ea92b"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16571-402-10)", "package_ndc": "16571-402-10", "marketing_start_date": "20091001"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (16571-402-50)", "package_ndc": "16571-402-50", "marketing_start_date": "20091001"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "16571-402_76ebe5e7-afda-45c3-bf06-07e37827a07a", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "16571-402", "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": "10 mg/1"}], "application_number": "ANDA077829", "marketing_category": "ANDA", "marketing_start_date": "20091001", "listing_expiration_date": "20261231"}