# gemcitabine

NDC: 55111-686
Generic name: gemcitabine
Labeler / Manufacturer: Dr. Reddy's Laboratories Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20110725

FDA application: ANDA091365

## Active ingredients

- GEMCITABINE HYDROCHLORIDE: 200 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55111-686"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55111-686
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=eafcebc8-ddef-bb6b-fd0a-9d8b9962cdc4