Package 55111-687-25

Brand: gemcitabine

Generic: gemcitabine
NDC Package

Package Facts

Identity

Package NDC 55111-687-25
Digits Only 5511168725
Product NDC 55111-687
Description

1 VIAL, SINGLE-USE in 1 CARTON (55111-687-25) / 25 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2011-07-25
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": "12d7e1d6-334a-7d1c-2db2-ea73c496d9ff", "openfda": {"unii": ["U347PV74IL"], "rxcui": ["1719000", "1719003"], "spl_set_id": ["eafcebc8-ddef-bb6b-fd0a-9d8b9962cdc4"], "manufacturer_name": ["Dr. Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (55111-687-25)  / 25 mL in 1 VIAL, SINGLE-USE", "package_ndc": "55111-687-25", "marketing_start_date": "20110725"}], "brand_name": "gemcitabine", "product_id": "55111-687_12d7e1d6-334a-7d1c-2db2-ea73c496d9ff", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Nucleic Acid Synthesis Inhibitors [MoA]", "Nucleoside Metabolic Inhibitor [EPC]"], "product_ndc": "55111-687", "generic_name": "gemcitabine", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "gemcitabine", "active_ingredients": [{"name": "GEMCITABINE HYDROCHLORIDE", "strength": "1 g/25mL"}], "application_number": "ANDA091365", "marketing_category": "ANDA", "marketing_start_date": "20110725", "listing_expiration_date": "20261231"}