Package 0409-0183-01

Brand: gemcitabine

Generic: gemcitabine
NDC Package

Package Facts

Identity

Package NDC 0409-0183-01
Digits Only 0409018301
Product NDC 0409-0183
Product ID 0409-0183_949ef588-ec7f-4dce-964e-984cd6618423
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0183-01) / 5.26 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2011-08-24
Brand gemcitabine
Generic gemcitabine
Sample Package No

Linked Drug Pages (1)

Gemcitabine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "949ef588-ec7f-4dce-964e-984cd6618423", "openfda": {"unii": ["U347PV74IL"], "rxcui": ["1720960", "1720975", "1720977"], "spl_set_id": ["dc02a23b-3ff9-4441-aa91-8e9e629a7315"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0183-01)  / 5.26 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0409-0183-01", "marketing_start_date": "20110824"}], "brand_name": "Gemcitabine", "product_id": "0409-0183_949ef588-ec7f-4dce-964e-984cd6618423", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Nucleic Acid Synthesis Inhibitors [MoA]", "Nucleoside Metabolic Inhibitor [EPC]"], "product_ndc": "0409-0183", "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": "20110824", "listing_expiration_date": "20261231"}