# Gemcitabine

NDC: 0409-0183
Generic name: GEMCITABINE
Labeler / Manufacturer: Hospira, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20130709

FDA application: NDA200795

## Active ingredients

- GEMCITABINE HYDROCHLORIDE: 38 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0409-0183"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-0183
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e18ed1cb-7dd0-4001-bfda-17d1f4587fb8