Orange Book product · Generic (ANDA)
SELEGILINE HYDROCHLORIDE
SELEGILINE HYDROCHLORIDE
At a glance
Apr 01, 1997
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Apr 01, 1997
29 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
SELEGILINE HYDROCHLORIDE
Strength
5MG
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 074672
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of SELEGILINE HYDROCHLORIDE
- 2006ZELAPARBrand (NDA)
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NDA 020647 · QUAGEN
- 1989SELEGILINE HYDROCHLORIDEBrand (NDA)
NDA 019334 · QUAGEN
- 2019SELEGILINE HYDROCHLORIDEGeneric (ANDA)
ANDA 206803 · RISING
- 2003SELEGILINE HYDROCHLORIDEGeneric (ANDA)
ANDA 075145 · LANNETT CO INC
- 1998SELEGILINE HYDROCHLORIDEGeneric (ANDA)
ANDA 075321 · APOTEX
- 1998SELEGILINE HYDROCHLORIDEGeneric (ANDA)
ANDA 075352 · NOVITIUM PHARMA
- 1998SELEGILINE HYDROCHLORIDEGeneric (ANDA)
ANDA 074756 · COSETTE
- 1998SELEGILINE HYDROCHLORIDEGeneric (ANDA)
ANDA 074912 · KENTON
- 1997SELEGILINE HYDROCHLORIDEGeneric (ANDA)
ANDA 074866 · NOVITIUM PHARMA
- 1997SELEGILINE HYDROCHLORIDEGeneric (ANDA)
ANDA 074871 · APOTEX
- 1997SELEGILINE HYDROCHLORIDEGeneric (ANDA)
ANDA 074744 · COSETTE
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.
