Orange Book product · Generic (ANDA)
NANDROLONE PHENPROPIONATE
NANDROLONE PHENPROPIONATE
Generic (ANDA)ANDA 087488DISCN WATSON LABS
At a glance
Jun 17, 1983
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jun 17, 1983
43 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
NANDROLONE PHENPROPIONATE
Strength
50MG/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
ANDA 087488
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of NANDROLONE PHENPROPIONATE
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
