Package 0904-6552-61

Brand: ondansetron

Generic: ondansetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-6552-61
Digits Only 0904655261
Product NDC 0904-6552
Product ID 0904-6552_50aa5f42-2197-43a5-836a-4e0c96209a8b
Description

100 BLISTER PACK in 1 CARTON (0904-6552-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2006-12-26
Brand ondansetron
Generic ondansetron hydrochloride
Sample Package No

Linked Drug Pages (1)

ondansetron ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "50aa5f42-2197-43a5-836a-4e0c96209a8b", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["198052", "312086"], "spl_set_id": ["a29b5c18-9884-4c88-8827-65d9ad5f69f6"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6552-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6552-61", "marketing_start_date": "20061226"}], "brand_name": "ondansetron", "product_id": "0904-6552_50aa5f42-2197-43a5-836a-4e0c96209a8b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "0904-6552", "generic_name": "ondansetron hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ondansetron", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "8 mg/1"}], "application_number": "ANDA076183", "marketing_category": "ANDA", "marketing_start_date": "20061226", "listing_expiration_date": "20261231"}