The U.S. Food and Drug Administration (FDA) has recorded a regulatory status change for a topical product containing hydrocortisone. The product, identified as HYDROCORTISONE 0.5% OINTMENT (product number 003), is manufactured by Perrigo New York. According to the FDA’s database, the product is classified as a non‑reference drug and is now marked as "Discontinued" under the Abbreviated New Drug Application (ANDA) number ANDA084969. No reference standard is associated with this submission.
Key details:
- Route: Topical
- Dosage form: Ointment
- Active ingredient: Hydrocortisone 0.5%
- Sponsor: Perrigo New York
- Marketing status: Discontinued
- Application number: ANDA084969
Actualités réglementaires28 sept. 2026•1 min de lecture
FDA Discontinues Hydrocortisone 0.5% Ointment (ANDA084969)
The FDA has listed the hydrocortisone 0.5% topical ointment (product 003) from Perrigo New York as discontinued under application ANDA084969.
Compilé par l'équipe PharmaCountry · Source : FDA.gov
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