# Baclofen

NDC: 16714-072
Generic name: Baclofen
Labeler / Manufacturer: Northstar RxLLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20110101

FDA application: ANDA078401

## Active ingredients

- BACLOFEN: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16714-072"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16714-072
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0aac77fa-30c2-46c8-a04d-e6b8333ddd81