Package 71141-133-32

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71141-133-32
Digits Only 7114113332
Product NDC 71141-133
Product ID 71141-133_4cf9e5b8-0be6-4a8b-9ee3-7e7272864279
Description

1 BLISTER PACK in 1 CARTON (71141-133-32) / 14 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2017-09-01
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": "4cf9e5b8-0be6-4a8b-9ee3-7e7272864279", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["a210d6b7-0829-4120-bb6d-fee0c2e57b26"], "manufacturer_name": ["LIDL US, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (71141-133-32)  / 14 TABLET in 1 BLISTER PACK", "package_ndc": "71141-133-32", "marketing_start_date": "20170901"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "71141-133_4cf9e5b8-0be6-4a8b-9ee3-7e7272864279", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "71141-133", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "LIDL US, LLC", "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": "20170901", "listing_expiration_date": "20261231"}