Orange Book product · Brand (NDA)
LUDIOMIL
MAPROTILINE HYDROCHLORIDE
At a glance
Approved Prior to Jan 1, 1982
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
No patent or exclusivity dates are listed for this product.
Pharmaceutical detail
Active ingredient
MAPROTILINE HYDROCHLORIDE
Strength
25MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
NDA 017543
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a brand (NDA) product. Other products sharing this active ingredient are listed below.
- 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 072129 · AM THERAP
- 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.
