Acticort

ANDA 86535, held by Baker Norton. Hydrocortisone.

As of Nov 13, 2026, ANDA 86535 (Acticort), held by Baker Norton, was first approved by FDA on Feb 4, 1981, with 1 approved supplement and 0 published complete response letters.

First approved: Feb 4, 1981
Supplements approved: 1
Complete response letters: 0

Approvals and New Uses

The original application and every efficacy supplement, newest first; all 2 submissions below

Date	Submission	Status	Documents
Feb 4, 1981	Original application	Approved	None posted

Products

1 strengths and forms

Product	Active ingredient	Marketing
Acticort1% · lotion;topical	Hydrocortisone	Discontinued

All 2 submissions, including labeling and manufacturing supplements


May 22, 1984	Supplement 2Manufacturing	Approved	None posted
Feb 4, 1981	Original application	Approved	None posted

Identifiers

Application: ANDA 86535
Drugs@FDA: Overview at FDA
Company: Baker Norton Pharmaceuticals

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