Package 0781-5284-64
Brand: cetirizine hydrochloride
Generic: cetirizine hydrochloridePackage Facts
Identity
Package NDC
0781-5284-64
Digits Only
0781528464
Product NDC
0781-5284
Description
30 BLISTER PACK in 1 CARTON (0781-5284-64) / 1 TABLET, CHEWABLE in 1 BLISTER PACK (0781-5284-06)
Marketing
Marketing Status
Brand
cetirizine hydrochloride
Generic
cetirizine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6b525723-7253-44e7-af75-f409b3ec77c2", "openfda": {"upc": ["0307815284640"], "unii": ["64O047KTOA"], "rxcui": ["1014674"], "spl_set_id": ["a814a06b-96ed-4403-bbd7-fc1142988b50"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0781-5284-64) / 1 TABLET, CHEWABLE in 1 BLISTER PACK (0781-5284-06)", "package_ndc": "0781-5284-64", "marketing_start_date": "20080214"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "0781-5284_6b525723-7253-44e7-af75-f409b3ec77c2", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0781-5284", "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": "ANDA078692", "marketing_category": "ANDA", "marketing_start_date": "20080214", "listing_expiration_date": "20261231"}