Orange Book product · Generic (ANDA)
FINASTERIDE
FINASTERIDE
At a glance
Mar 28, 2007
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Mar 28, 2007
19 yr 6 mo ago
Today
Pharmaceutical detail
Active ingredient
FINASTERIDE
Strength
5MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 077914
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of FINASTERIDE
- 1997PROPECIABrand (NDA)
NDA 020788 · ORGANON
- 1992PROSCARBrand (NDA)
NDA 020180 · ORGANON
- 2017FINASTERIDEGeneric (ANDA)
ANDA 207750 · ALKEM LABS LTD
- 2017FINASTERIDEGeneric (ANDA)
ANDA 204304 · ALKEM LABS LTD
- 2014FINASTERIDEGeneric (ANDA)
ANDA 077335 · CIPLA
- 2013FINASTERIDEGeneric (ANDA)
ANDA 091643 · ACCORD HLTHCARE
- 2013FINASTERIDEGeneric (ANDA)
ANDA 078371 · ACTAVIS TOTOWA
- 2013FINASTERIDEGeneric (ANDA)
ANDA 203687 · AUROBINDO PHARMA LTD
- 2013FINASTERIDEGeneric (ANDA)
ANDA 078161 · NATCO PHARMA
- 2013FINASTERIDEGeneric (ANDA)
ANDA 076905 · TEVA
- 2013FINASTERIDEGeneric (ANDA)
ANDA 090060 · HETERO LABS LTD III
- 2013FINASTERIDEGeneric (ANDA)
ANDA 090508 · SUN PHARM
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.
