Package 63304-458-30

Brand: ondansetron

Generic: ondansetron
NDC Package

Package Facts

Identity

Package NDC 63304-458-30
Digits Only 6330445830
Product NDC 63304-458
Product ID 63304-458_ad113c32-f57c-4548-9882-c46b9a990bd8
Description

30 TABLET, FILM COATED in 1 BOTTLE (63304-458-30)

Marketing

Marketing Status
Marketed Since 2007-06-25
Brand ondansetron
Generic ondansetron
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": "ad113c32-f57c-4548-9882-c46b9a990bd8", "openfda": {"upc": ["0363304458305", "0363304459302"], "unii": ["NMH84OZK2B"], "rxcui": ["198052", "312086"], "spl_set_id": ["834bc56a-657d-4733-9a60-47040cb5c7bf"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63304-458-30)", "package_ndc": "63304-458-30", "marketing_start_date": "20070625"}], "brand_name": "ONDANSETRON", "product_id": "63304-458_ad113c32-f57c-4548-9882-c46b9a990bd8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "63304-458", "generic_name": "ONDANSETRON", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ONDANSETRON", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA077851", "marketing_category": "ANDA", "marketing_start_date": "20070625", "listing_expiration_date": "20261231"}