Relieves inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses…. ANDA 215832, held by Alembic. Betamethasone Valerate.
As of Nov 15, 2026, ANDA 215832 (Betamethasone Valerate), held by Alembic, was first approved by FDA on Aug 22, 2024, with 0 approved supplements and 0 published complete response letters.
INDICATIONS AND USAGE Betamethasone valerate foam, 0.12% is a medium potency topical corticosteroid indicated for relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses of the scalp.
| Date | Submission | Status | Documents |
|---|---|---|---|
| Aug 22, 2024 | Original application | Approved | None posted |
| Product | Active ingredient | Marketing |
|---|---|---|
| Betamethasone Valerate0.12% · aerosol, foam;topical | Betamethasone Valerate | Rx |
Approvals, supplements, products and documents come from FDA's Drugs@FDA data files, refreshed daily; Drugs@FDA lists approved applications only. Complete response letters are FDA's published letters. Drugs@FDA and FDA complete response letters
