# Cambia

NDC: 13913-012
Generic name: diclofenac potassium
Labeler / Manufacturer: Assertio Therapeutics, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: POWDER, FOR SOLUTION
Routes: ORAL
Marketing started: 20160310

FDA application: NDA022165

## Active ingredients

- DICLOFENAC POTASSIUM: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"13913-012"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=13913-012
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d249ced1-4ca0-4f57-adcb-23440f58f659