# Diclofenac potassium

NDC: 0480-9435
Generic name: diclofenac potassium
Labeler / Manufacturer: TEVA PHARMACEUTICALS, INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, LIQUID FILLED
Routes: ORAL
Marketing started: 20220324

FDA application: ANDA204648

## Active ingredients

- DICLOFENAC POTASSIUM: 25 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0480-9435"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0480-9435
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d9685883-9d0b-81da-e053-2a95a90ab8d8
