Package 60760-886-30

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-886-30
Digits Only 6076088630
Product NDC 60760-886
Product ID 60760-886_4536b98f-f486-7cd9-e063-6394a90a2f5d
Description

30 TABLET in 1 BOTTLE, PLASTIC (60760-886-30)

Marketing

Marketing Status
Marketed Since 2023-01-17
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": "4536b98f-f486-7cd9-e063-6394a90a2f5d", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["f2f42f36-6b09-4140-e053-2a95a90af813"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (60760-886-30)", "package_ndc": "60760-886-30", "marketing_start_date": "20230117"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "60760-886_4536b98f-f486-7cd9-e063-6394a90a2f5d", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "60760-886", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "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": "20230117", "listing_expiration_date": "20261231"}