FDA — authorised 12 June 1941
- Application: NDA003977
- Marketing authorisation holder: PARKEDALE
- Local brand name: THEELIN
- Indication: INJECTABLE — INJECTION
- Status: approved
🇺🇸 Skin test panel and desensitization kit in United States
FDA authorised Skin test panel and desensitization kit on 12 June 1941
Marketing authorisations
FDA — authorised 21 February 1979
- Application: ANDA085239
- Marketing authorisation holder: DR REDDYS
- Local brand name: ESTRONE
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA
- Application: ANDA083397
- Marketing authorisation holder: WATSON LABS
- Local brand name: ESTRONE
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA
- Application: ANDA083488
- Marketing authorisation holder: WYETH AYERST
- Local brand name: ESTROGENIC SUBSTANCE
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA
- Application: ANDA085237
- Marketing authorisation holder: WATSON LABS
- Local brand name: NATURAL ESTROGENIC SUBSTANCE-ESTRONE
- Indication: INJECTABLE — INJECTION
- Status: approved
Frequently asked questions
Is Skin test panel and desensitization kit approved in United States?
Yes. FDA authorised it on 12 June 1941; FDA authorised it on 21 February 1979; FDA has authorised it.
Who is the marketing authorisation holder for Skin test panel and desensitization kit in United States?
PARKEDALE holds the US marketing authorisation.