Package 68071-1742-3
Brand: ondansetron hydrochloride
Generic: ondansetron hydrochloridePackage Facts
Identity
Package NDC
68071-1742-3
Digits Only
6807117423
Product NDC
68071-1742
Description
30 TABLET, FILM COATED in 1 BOTTLE (68071-1742-3)
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": "2d82d4f9-ca65-ed20-e063-6294a90aacf4", "openfda": {"upc": ["0368071174236"], "unii": ["NMH84OZK2B"], "rxcui": ["312086"], "spl_set_id": ["f8ada0e4-5c1b-17ab-e053-6294a90a12b8"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-1742-3)", "package_ndc": "68071-1742-3", "marketing_start_date": "20230406"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "68071-1742_2d82d4f9-ca65-ed20-e063-6294a90aacf4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "68071-1742", "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": "8 mg/1"}], "application_number": "ANDA078539", "marketing_category": "ANDA", "marketing_start_date": "20070731", "listing_expiration_date": "20261231"}