🇺🇸 Nandrolone Decanoate in United States

FDA authorised Nandrolone Decanoate on 5 October 1962

Marketing authorisations

FDA — authorised 5 October 1962

  • Marketing authorisation holder: ASPEN GLOBAL INC
  • Status: approved

FDA — authorised 5 October 1962

  • Application: NDA013132
  • Marketing authorisation holder: WOODWARD SPECL
  • Local brand name: DECA-DURABOLIN
  • Indication: INJECTABLE — INJECTION
  • Status: approved

Read official source →

FDA — authorised 17 May 1983

  • Application: ANDA086385
  • Marketing authorisation holder: WATSON LABS
  • Local brand name: NANDROLONE DECANOATE
  • Indication: INJECTABLE — INJECTION
  • Status: approved

Read official source →

FDA — authorised 17 May 1983

  • Application: ANDA086598
  • Marketing authorisation holder: WATSON LABS
  • Local brand name: NANDROLONE DECANOATE
  • Indication: INJECTABLE — INJECTION
  • Status: approved

Read official source →

FDA — authorised 14 October 1983

  • Application: ANDA088317
  • Marketing authorisation holder: ABRAXIS PHARM
  • Local brand name: NANDROLONE DECANOATE
  • Indication: INJECTABLE — INJECTION
  • Status: approved

Read official source →

FDA — authorised 5 December 1983

  • Application: ANDA088128
  • Marketing authorisation holder: WATSON LABS
  • Local brand name: NANDROLONE DECANOATE
  • Indication: INJECTABLE — INJECTION
  • Status: approved

Read official source →

FDA — authorised 17 March 1989

  • Application: ANDA088290
  • Marketing authorisation holder: ABRAXIS PHARM
  • Local brand name: NANDROLONE DECANOATE
  • Indication: INJECTABLE — INJECTION
  • Status: approved

Read official source →

FDA — authorised 30 August 2010

  • Application: ANDA091252
  • Marketing authorisation holder: AM REGENT
  • Local brand name: NANDROLONE DECANOATE
  • Indication: INJECTABLE — INJECTION
  • Status: approved

Read official source →

FDA

  • Application: ANDA089249
  • Marketing authorisation holder: QUAD PHARMS
  • Local brand name: NANDROLONE DECANOATE
  • Indication: Injectable — Injection
  • Status: approved

Read official source →

FDA

  • Application: ANDA089248
  • Marketing authorisation holder: QUAD PHARMS
  • Local brand name: NANDROLONE DECANOATE
  • Indication: Injectable — Injection
  • Status: approved

Read official source →

FDA

  • Application: ANDA089250
  • Marketing authorisation holder: QUAD PHARMS
  • Local brand name: NANDROLONE DECANOATE
  • Indication: Injectable — Injection
  • Status: approved

Read official source →

FDA

  • Application: ANDA088554
  • Marketing authorisation holder: WATSON LABS
  • Local brand name: NANDROLONE DECANOATE
  • Indication: INJECTABLE — INJECTION
  • Status: approved

Read official source →

FDA

  • Application: ANDA087519
  • Marketing authorisation holder: EPIC PHARMA LLC
  • Local brand name: NANDROLONE DECANOATE
  • Indication: INJECTABLE — INJECTION
  • Status: approved

Read official source →

FDA

  • Application: ANDA087598
  • Marketing authorisation holder: WATSON LABS
  • Local brand name: NANDROLONE DECANOATE
  • Indication: INJECTABLE — INJECTION
  • Status: approved

Read official source →

FDA

  • Application: ANDA087599
  • Marketing authorisation holder: WATSON LABS
  • Local brand name: NANDROLONE DECANOATE
  • Indication: INJECTABLE — INJECTION
  • Status: approved

Read official source →

Nandrolone Decanoate in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Other Hematology approved in United States

Frequently asked questions

Is Nandrolone Decanoate approved in United States?

Yes. FDA authorised it on 5 October 1962; FDA authorised it on 5 October 1962; FDA authorised it on 17 May 1983.

Who is the marketing authorisation holder for Nandrolone Decanoate in United States?

ASPEN GLOBAL INC holds the US marketing authorisation.