Package 51672-4091-3

Brand: ondansetron

Generic: ondansetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51672-4091-3
Digits Only 5167240913
Product NDC 51672-4091
Description

1 BOTTLE in 1 CARTON (51672-4091-3) / 50 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2007-11-30
Brand ondansetron
Generic ondansetron hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e10032ef-6d48-44cb-9b7f-9a338f35ca51", "openfda": {"upc": ["0351672409135"], "unii": ["NMH84OZK2B"], "rxcui": ["312085"], "spl_set_id": ["a95ca4f4-c4de-4822-9a08-209d10bf5136"], "manufacturer_name": ["Taro Pharmaceuticals U.S.A., Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (51672-4091-3)  / 50 mL in 1 BOTTLE", "package_ndc": "51672-4091-3", "marketing_start_date": "20071130"}], "brand_name": "Ondansetron", "product_id": "51672-4091_e10032ef-6d48-44cb-9b7f-9a338f35ca51", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "51672-4091", "generic_name": "ondansetron hydrochloride", "labeler_name": "Taro Pharmaceuticals U.S.A., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "4 mg/5mL"}], "application_number": "ANDA077009", "marketing_category": "ANDA", "marketing_start_date": "20071130", "listing_expiration_date": "20261231"}