Package 68071-5047-3
Brand: ondansetron hydrochloride
Generic: ondansetron hydrochloridePackage Facts
Identity
Package NDC
68071-5047-3
Digits Only
6807150473
Product NDC
68071-5047
Description
30 TABLET, FILM COATED in 1 BOTTLE (68071-5047-3)
Marketing
Marketing Status
Brand
ondansetron hydrochloride
Generic
ondansetron hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b418113-cac0-842f-e063-6294a90a71fa", "openfda": {"upc": ["0368071504736"], "unii": ["NMH84OZK2B"], "rxcui": ["198052"], "spl_set_id": ["91bfbc0e-86a3-8ac6-e053-2a95a90af432"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-5047-3)", "package_ndc": "68071-5047-3", "marketing_start_date": "20190904"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "68071-5047_1b418113-cac0-842f-e063-6294a90a71fa", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "68071-5047", "generic_name": "Ondansetron Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron Hydrochloride", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA078539", "marketing_category": "ANDA", "marketing_start_date": "20070731", "listing_expiration_date": "20261231"}