Orange Book product · Generic (ANDA)
MAPROTILINE HYDROCHLORIDE
MAPROTILINE HYDROCHLORIDE
At a glance
Jan 14, 1988
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 14, 1988
39 yr ago
Today
Pharmaceutical detail
Active ingredient
MAPROTILINE HYDROCHLORIDE
Strength
25MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 072129
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of MAPROTILINE HYDROCHLORIDE
- —LUDIOMILBrand (NDA)
NDA 017543 · NOVARTIS
- 1988MAPROTILINE HYDROCHLORIDEGeneric (ANDA)
ANDA 072285 · RISING
- 1988MAPROTILINE HYDROCHLORIDEGeneric (ANDA)
ANDA 072162 · HERITAGE PHARMA
- 1988MAPROTILINE HYDROCHLORIDEGeneric (ANDA)
ANDA 072163 · HERITAGE PHARMA
- 1988MAPROTILINE HYDROCHLORIDEGeneric (ANDA)
ANDA 072164 · WATSON LABS
- 1988MAPROTILINE HYDROCHLORIDEGeneric (ANDA)
ANDA 072130 · AM THERAP
- 1988MAPROTILINE HYDROCHLORIDEGeneric (ANDA)
ANDA 072131 · AM THERAP
- 1987MAPROTILINE HYDROCHLORIDEGeneric (ANDA)
ANDA 071943 · WATSON LABS
- 1987MAPROTILINE HYDROCHLORIDEGeneric (ANDA)
ANDA 071944 · WATSON LABS
- 1987MAPROTILINE HYDROCHLORIDEGeneric (ANDA)
ANDA 071945 · WATSON LABS
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.
