Details for New Drug Application (NDA): 071943
NDA 071943 describes MAPROTILINE HYDROCHLORIDE, which is a drug marketed by Am Therap, Heritage Pharma, Rising, and Watson Labs, and is included in ten NDAs. Additional details are available on the MAPROTILINE HYDROCHLORIDE profile page.
The generic ingredient in MAPROTILINE HYDROCHLORIDE is maprotiline hydrochloride. There is one drug master file entry for this compound. Additional details are available on the maprotiline hydrochloride profile page.
The generic ingredient in MAPROTILINE HYDROCHLORIDE is maprotiline hydrochloride. There is one drug master file entry for this compound. Additional details are available on the maprotiline hydrochloride profile page.
Summary for 071943
| Tradename: | MAPROTILINE HYDROCHLORIDE |
| Applicant: | Watson Labs |
| Ingredient: | maprotiline hydrochloride |
| Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 071943
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 25MG | ||||
| Approval Date: | Dec 30, 1987 | TE: | RLD: | No | |||||
Complete Access Available with Subscription
