Package 0409-0182-25

Brand: gemcitabine

Generic: gemcitabine
NDC Package

Package Facts

Identity

Package NDC 0409-0182-25
Digits Only 0409018225
Product NDC 0409-0182
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0182-25) / 52.6 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2013-07-29
Brand gemcitabine
Generic gemcitabine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "15f70b30-31dc-4c45-902b-69cad93f7308", "openfda": {"unii": ["U347PV74IL"], "rxcui": ["1720960", "1720975", "1720977"], "spl_set_id": ["e18ed1cb-7dd0-4001-bfda-17d1f4587fb8"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0182-25)  / 52.6 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0409-0182-25", "marketing_start_date": "20130729"}], "brand_name": "Gemcitabine", "product_id": "0409-0182_15f70b30-31dc-4c45-902b-69cad93f7308", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Nucleic Acid Synthesis Inhibitors [MoA]", "Nucleoside Metabolic Inhibitor [EPC]"], "product_ndc": "0409-0182", "generic_name": "GEMCITABINE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gemcitabine", "active_ingredients": [{"name": "GEMCITABINE HYDROCHLORIDE", "strength": "38 mg/mL"}], "application_number": "NDA200795", "marketing_category": "NDA", "marketing_start_date": "20130729", "listing_expiration_date": "20261231"}