Package 16714-159-01

Brand: ondansetron

Generic: ondansetron
NDC Package

Package Facts

Identity

Package NDC 16714-159-01
Digits Only 1671415901
Product NDC 16714-159
Description

30 TABLET, FILM COATED in 1 BOTTLE (16714-159-01)

Marketing

Marketing Status
Marketed Since 2021-04-06
Brand ondansetron
Generic ondansetron
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9e8d8ea3-cbef-49ef-bcda-3ae6b9ea68d1", "openfda": {"upc": ["0316714160016", "0316714159010"], "unii": ["NMH84OZK2B"], "rxcui": ["198052", "312086"], "spl_set_id": ["9d5e7650-95be-4b96-b29c-374f673eb7a1"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (16714-159-01)", "package_ndc": "16714-159-01", "marketing_start_date": "20210406"}], "brand_name": "Ondansetron", "product_id": "16714-159_9e8d8ea3-cbef-49ef-bcda-3ae6b9ea68d1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "16714-159", "generic_name": "Ondansetron", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA078539", "marketing_category": "ANDA", "marketing_start_date": "20210406", "listing_expiration_date": "20261231"}