Package 0781-1684-64

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0781-1684-64
Digits Only 0781168464
Product NDC 0781-1684
Product ID 0781-1684_2ca4b053-0031-4a34-a1b1-8eaadb0879c6
Description

30 TABLET in 1 BOX, UNIT-DOSE (0781-1684-64)

Marketing

Marketing Status
Marketed Since 2007-12-27
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": "2ca4b053-0031-4a34-a1b1-8eaadb0879c6", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["760dd0e4-280a-4d95-8938-cecaa7ec75f2"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0781-1684-01)", "package_ndc": "0781-1684-01", "marketing_start_date": "20071227"}, {"sample": false, "description": "30 TABLET in 1 BOX, UNIT-DOSE (0781-1684-64)", "package_ndc": "0781-1684-64", "marketing_start_date": "20071227"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "0781-1684_2ca4b053-0031-4a34-a1b1-8eaadb0879c6", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0781-1684", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077946", "marketing_category": "ANDA", "marketing_start_date": "20071227", "listing_expiration_date": "20261231"}