drugmine

molindone-hydrochloride


Name: MOLINDONE HYDROCHLORIDE
ID :
MW: 276
Number of atoms: 20
Molecular_Formula: C16H24N2O2
Alogp: 2.14
Indication class : Antipsychotic
Oral Flag : 1
Max_Phase : 4
Molecule_Type : Small molecule

molindone hydrochloride containing products summary

There are in total 9 different products containing the active ingredient molindone hydrochloride. From the 9 drug products, 9 have been discontinued.

Product id = 2539
Application Number = 17111
Date of Application = Prior, Approved, to
RX/OTC/DISCN = DISCN
Tradename = MOBAN
Route/format = ORAL / CAPSULE
Application Type = N
Applicant Name = ENDO PHARMS
ProductNo = 001
Tecode =
Rld = No
Strength = 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
----
Product id = 2540
Application Number = 17111
Date of Application = Prior, Approved, to
RX/OTC/DISCN = DISCN
Tradename = MOBAN
Route/format = ORAL / CAPSULE
Application Type = N
Applicant Name = ENDO PHARMS
ProductNo = 002
Tecode =
Rld = No
Strength = 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
----
Product id = 2541
Application Number = 17111
Date of Application = Prior, Approved, to
RX/OTC/DISCN = DISCN
Tradename = MOBAN
Route/format = ORAL / CAPSULE
Application Type = N
Applicant Name = ENDO PHARMS
ProductNo = 003
Tecode =
Rld = No
Strength = 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
----
Product id = 25021
Application Number = 17111
Date of Application = Prior, Approved, to
RX/OTC/DISCN = DISCN
Tradename = MOBAN
Route/format = ORAL / TABLET
Application Type = N
Applicant Name = ENDO PHARMS
ProductNo = 004
Tecode =
Rld = No
Strength = 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
----
Product id = 25022
Application Number = 17111
Date of Application = Prior, Approved, to
RX/OTC/DISCN = DISCN
Tradename = MOBAN
Route/format = ORAL / TABLET
Application Type = N
Applicant Name = ENDO PHARMS
ProductNo = 005
Tecode =
Rld = No
Strength = 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
----
Product id = 25023
Application Number = 17111
Date of Application = Prior, Approved, to
RX/OTC/DISCN = DISCN
Tradename = MOBAN
Route/format = ORAL / TABLET
Application Type = N
Applicant Name = ENDO PHARMS
ProductNo = 006
Tecode =
Rld = No
Strength = 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
----
Product id = 25024
Application Number = 17111
Date of Application = Prior, Approved, to
RX/OTC/DISCN = DISCN
Tradename = MOBAN
Route/format = ORAL / TABLET
Application Type = N
Applicant Name = ENDO PHARMS
ProductNo = 007
Tecode =
Rld = No
Strength = 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
----
Product id = 25025
Application Number = 17111
Date of Application = Prior, Approved, to
RX/OTC/DISCN = DISCN
Tradename = MOBAN
Route/format = ORAL / TABLET
Application Type = N
Applicant Name = ENDO PHARMS
ProductNo = 008
Tecode =
Rld = No
Strength = 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
----
Product id = 3954
Application Number = 17938
Date of Application = Prior, Approved, to
RX/OTC/DISCN = DISCN
Tradename = MOBAN
Route/format = ORAL / CONCENTRATE
Application Type = N
Applicant Name = ENDO PHARMS
ProductNo = 001
Tecode =
Rld = No
Strength = 20MG/ML
----