Package 51316-764-65

Brand: cetirizine

Generic: cetiirizine
NDC Package

Package Facts

Identity

Package NDC 51316-764-65
Digits Only 5131676465
Product NDC 51316-764
Product ID 51316-764_465428ca-3000-a730-e063-6394a90a1af4
Description

365 TABLET in 1 BOTTLE (51316-764-65)

Marketing

Marketing Status
Marketed Since 2023-10-16
Brand cetirizine
Generic cetiirizine
Sample Package No

Linked Drug Pages (1)

Cetirizine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "465428ca-3000-a730-e063-6394a90a1af4", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["fd8f495a-9940-363b-e053-6294a90a1097"], "manufacturer_name": ["CVS PHARMACY, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "365 TABLET in 1 BOTTLE (51316-764-65)", "package_ndc": "51316-764-65", "marketing_start_date": "20231016"}], "brand_name": "Cetirizine", "product_id": "51316-764_465428ca-3000-a730-e063-6394a90a1af4", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51316-764", "generic_name": "Cetiirizine", "labeler_name": "CVS PHARMACY, INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209274", "marketing_category": "ANDA", "marketing_start_date": "20231016", "listing_expiration_date": "20261231"}