Package 68071-4966-4

Brand: ondansetron hydrochloride

Generic: ondansetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-4966-4
Digits Only 6807149664
Product NDC 68071-4966
Description

4 TABLET, FILM COATED in 1 BOTTLE (68071-4966-4)

Marketing

Marketing Status
Marketed Since 2019-07-11
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": "1b2e68f9-41a8-bd88-e063-6294a90a08b5", "openfda": {"upc": ["0368071496642"], "unii": ["NMH84OZK2B"], "rxcui": ["312086"], "spl_set_id": ["8d696b8c-eba6-505e-e053-2995a90acb5d"], "manufacturer_name": ["NUCARE PHARMACEUTICALS INC"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE (68071-4966-4)", "package_ndc": "68071-4966-4", "marketing_start_date": "20190711"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "68071-4966_1b2e68f9-41a8-bd88-e063-6294a90a08b5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "68071-4966", "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"}