Details for New Drug Application (NDA): 040751
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NDA 040751 describes IMIPRAMINE HYDROCHLORIDE, which is a drug marketed by Novartis, Chartwell, Leading, Lederle, Oxford Pharms, Par Pharm, Roxane, Sandoz, Specgx Llc, Strides Pharma Intl, Sun Pharm Industries, Teva, Usl Pharma, Vangard, Watson Labs, and West Ward, and is included in thirty-six NDAs. It is available from eleven suppliers. Additional details are available on the IMIPRAMINE HYDROCHLORIDE profile page.
The generic ingredient in IMIPRAMINE HYDROCHLORIDE is imipramine hydrochloride. There are thirty-four drug master file entries for this compound. Eleven suppliers are listed for this compound. Additional details are available on the imipramine hydrochloride profile page.
The generic ingredient in IMIPRAMINE HYDROCHLORIDE is imipramine hydrochloride. There are thirty-four drug master file entries for this compound. Eleven suppliers are listed for this compound. Additional details are available on the imipramine hydrochloride profile page.
Summary for 040751
| Tradename: | IMIPRAMINE HYDROCHLORIDE |
| Applicant: | Oxford Pharms |
| Ingredient: | imipramine hydrochloride |
| Patents: | 0 |
Suppliers and Packaging for NDA: 040751
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| IMIPRAMINE HYDROCHLORIDE | imipramine hydrochloride | TABLET;ORAL | 040751 | ANDA | NuCare Pharmaceuticals, Inc. | 68071-3669 | 68071-3669-9 | 90 TABLET in 1 BOTTLE (68071-3669-9) |
| IMIPRAMINE HYDROCHLORIDE | imipramine hydrochloride | TABLET;ORAL | 040751 | ANDA | Oxford Pharmaceuticals, LLC | 69584-425 | 69584-425-10 | 100 TABLET in 1 BOTTLE (69584-425-10) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 50MG | ||||
| Approval Date: | Feb 28, 2008 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 25MG | ||||
| Approval Date: | Feb 28, 2008 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
| Approval Date: | Feb 28, 2008 | TE: | AB | RLD: | No | ||||
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