# Pramosone

NDC: 54766-729
Generic name: hydrocortisone acetate and pramoxine hydrochloride
Labeler / Manufacturer: Sebela Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: LOTION
Routes: TOPICAL
Marketing started: 20150702
Marketing ended: 20261231
FDA application: ANDA085980

## Active ingredients

- HYDROCORTISONE ACETATE: 10 mg/mL
- PRAMOXINE HYDROCHLORIDE: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"54766-729"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=54766-729
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f207bdff-2f41-4eee-818e-198b6462863e