Package 68998-939-30

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68998-939-30
Digits Only 6899893930
Product NDC 68998-939
Product ID 68998-939_1e5b54b1-a7d9-44ae-b2e5-0a77793ad13a
Description

30 TABLET in 1 BOTTLE (68998-939-30)

Marketing

Marketing Status
Marketed Since 2012-11-01
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": "1e5b54b1-a7d9-44ae-b2e5-0a77793ad13a", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["f30900e6-425f-43e0-81b6-1fa3bd321f0b"], "manufacturer_name": ["Marc Glassman, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68998-939-30)", "package_ndc": "68998-939-30", "marketing_start_date": "20121101"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "68998-939_1e5b54b1-a7d9-44ae-b2e5-0a77793ad13a", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68998-939", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Marc Glassman, Inc.", "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": "20121101", "listing_expiration_date": "20261231"}