Package 0409-0187-01
Brand: gemcitabine
Generic: gemcitabinePackage Facts
Identity
Package NDC
0409-0187-01
Digits Only
0409018701
Product NDC
0409-0187
Description
1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0187-01) / 50 mL in 1 VIAL, SINGLE-DOSE
Marketing
Marketing Status
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": "9788e02c-b92a-4ec3-a747-1574a3a76918", "openfda": {"unii": ["U347PV74IL"], "rxcui": ["1719005"], "spl_set_id": ["a625c92b-c569-4b98-8d2e-2b3f5e12b34f"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0187-01) / 50 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0409-0187-01", "marketing_start_date": "20101115"}], "brand_name": "GEMCITABINE", "product_id": "0409-0187_9788e02c-b92a-4ec3-a747-1574a3a76918", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Nucleic Acid Synthesis Inhibitors [MoA]", "Nucleoside Metabolic Inhibitor [EPC]"], "product_ndc": "0409-0187", "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": "ANDA079183", "marketing_category": "ANDA", "marketing_start_date": "20101115", "listing_expiration_date": "20261231"}