Package 63850-0004-1

Brand: ondansetron

Generic: ondansetron tablets
NDC Package

Package Facts

Identity

Package NDC 63850-0004-1
Digits Only 6385000041
Product NDC 63850-0004
Description

30 TABLET, FILM COATED in 1 BOTTLE (63850-0004-1)

Marketing

Marketing Status
Marketed Since 2007-06-25
Brand ondansetron
Generic ondansetron tablets
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "04819dac-e9c5-4d65-b8e4-15a1fd5a93c8", "openfda": {"upc": ["0363850000317"], "unii": ["NMH84OZK2B"], "rxcui": ["198052", "312086"], "spl_set_id": ["59c817b7-a1c6-48a5-9bfc-2c381532bfd9"], "manufacturer_name": ["Natco Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63850-0004-1)", "package_ndc": "63850-0004-1", "marketing_start_date": "20070625"}], "brand_name": "Ondansetron", "product_id": "63850-0004_04819dac-e9c5-4d65-b8e4-15a1fd5a93c8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "63850-0004", "generic_name": "Ondansetron Tablets", "labeler_name": "Natco Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "8 mg/1"}], "application_number": "ANDA077851", "marketing_category": "ANDA", "marketing_start_date": "20070625", "listing_expiration_date": "20261231"}