Package 25021-777-02

Brand: ondansetron

Generic: ondansetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 25021-777-02
Digits Only 2502177702
Product NDC 25021-777
Description

25 VIAL in 1 CARTON (25021-777-02) / 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2012-08-30
Brand ondansetron
Generic ondansetron hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "dbbafc2b-987e-421b-bcfc-d4706859420e", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["1740467"], "spl_set_id": ["ba0f8f13-1f7d-44e0-9c0f-0b43a9e8e3a7"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (25021-777-02)  / 2 mL in 1 VIAL", "package_ndc": "25021-777-02", "marketing_start_date": "20120830"}], "brand_name": "ondansetron", "product_id": "25021-777_dbbafc2b-987e-421b-bcfc-d4706859420e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "25021-777", "generic_name": "ondansetron hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ondansetron", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA079224", "marketing_category": "ANDA", "marketing_start_date": "20120830", "listing_expiration_date": "20261231"}