# Diclofenac Potassium

NDC: 49884-905
Generic name: Diclofenac Potassium
Labeler / Manufacturer: Endo USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SOLUTION
Routes: ORAL
Marketing started: 20230103

FDA application: ANDA202964

## 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:"49884-905"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49884-905
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2d45648f-cbea-41a4-8e3e-007b7bb7912c