Package 25021-235-51

Brand: gemcitabine

Generic: gemcitabine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 25021-235-51
Digits Only 2502123551
Product NDC 25021-235
Description

10 VIAL in 1 CARTON (25021-235-51) / 25 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2022-12-15
Brand gemcitabine
Generic gemcitabine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "595a8cf5-412a-482d-8d77-979741ee4912", "openfda": {"unii": ["U347PV74IL"], "rxcui": ["1719000", "1719003"], "spl_set_id": ["44bcc16c-341d-49e8-a1c6-95d084667aca"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (25021-235-50)  / 25 mL in 1 VIAL", "package_ndc": "25021-235-50", "marketing_start_date": "20141229"}, {"sample": false, "description": "10 VIAL in 1 CARTON (25021-235-51)  / 25 mL in 1 VIAL", "package_ndc": "25021-235-51", "marketing_start_date": "20221215"}], "brand_name": "gemcitabine", "product_id": "25021-235_595a8cf5-412a-482d-8d77-979741ee4912", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Nucleic Acid Synthesis Inhibitors [MoA]", "Nucleoside Metabolic Inhibitor [EPC]"], "product_ndc": "25021-235", "generic_name": "gemcitabine hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "gemcitabine", "active_ingredients": [{"name": "GEMCITABINE HYDROCHLORIDE", "strength": "1 g/25mL"}], "application_number": "ANDA202485", "marketing_category": "ANDA", "marketing_start_date": "20141229", "listing_expiration_date": "20261231"}