# Pramosone

NDC: 83107-021
Generic name: hydrocortisone acetate and pramoxine hydrochloride
Labeler / Manufacturer: Legacy Pharma USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: LOTION
Routes: TOPICAL
Marketing started: 20250527

FDA application: ANDA085979

## Active ingredients

- HYDROCORTISONE ACETATE: 25 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:"83107-021"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83107-021
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4c98a01e-ff11-45eb-8732-4bd9157969e8