Package 0781-5283-64
Brand: cetirizine hydrochloride
Generic: cetirizine hydrochloridePackage Facts
Identity
Package NDC
0781-5283-64
Digits Only
0781528364
Product NDC
0781-5283
Description
30 BLISTER PACK in 1 CARTON (0781-5283-64) / 1 TABLET, CHEWABLE in 1 BLISTER PACK (0781-5283-06)
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": "973d0d70-f69f-44b6-98f0-f436e63bd15a", "openfda": {"upc": ["0307815283643"], "unii": ["64O047KTOA"], "rxcui": ["1014643"], "spl_set_id": ["817d07cf-5e31-421f-9e95-943bae01f5b0"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0781-5283-64) / 1 TABLET, CHEWABLE in 1 BLISTER PACK (0781-5283-06)", "package_ndc": "0781-5283-64", "marketing_start_date": "20080214"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "0781-5283_973d0d70-f69f-44b6-98f0-f436e63bd15a", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0781-5283", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA078692", "marketing_category": "ANDA", "marketing_start_date": "20080214", "listing_expiration_date": "20261231"}