# GEMCITABINE

NDC: 68001-348
Generic name: GEMCITABINE
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20180525

FDA application: NDA209604

## Active ingredients

- GEMCITABINE HYDROCHLORIDE: 100 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-348"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-348
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4031017d-d768-46de-8081-476bcb883f5e