Details for New Drug Application (NDA): 072130
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The generic ingredient in MAPROTILINE HYDROCHLORIDE is maprotiline hydrochloride. There are three drug master file entries for this compound. Additional details are available on the maprotiline hydrochloride profile page.
Summary for 072130
Tradename: | MAPROTILINE HYDROCHLORIDE |
Applicant: | Am Therap |
Ingredient: | maprotiline hydrochloride |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Medical Subject Heading (MeSH) Categories for 072130
Profile for product number 001
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 50MG | ||||
Approval Date: | Jan 14, 1988 | TE: | RLD: | No |
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