Details for New Drug Application (NDA): 203293
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The generic ingredient in MEMANTINE HYDROCHLORIDE is donepezil hydrochloride; memantine hydrochloride. There are thirty-two drug master file entries for this compound. Six suppliers are listed for this compound. Additional details are available on the donepezil hydrochloride; memantine hydrochloride profile page.
Summary for 203293
| Tradename: | MEMANTINE HYDROCHLORIDE |
| Applicant: | Zydus Pharms |
| Ingredient: | memantine hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 203293
| Mechanism of Action | NMDA Receptor Antagonists |
Medical Subject Heading (MeSH) Categories for 203293
Suppliers and Packaging for NDA: 203293
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| MEMANTINE HYDROCHLORIDE | memantine hydrochloride | CAPSULE, EXTENDED RELEASE;ORAL | 203293 | ANDA | Zydus Pharmaceuticals USA Inc. | 68382-546 | 68382-546-06 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-546-06) |
| MEMANTINE HYDROCHLORIDE | memantine hydrochloride | CAPSULE, EXTENDED RELEASE;ORAL | 203293 | ANDA | Zydus Pharmaceuticals USA Inc. | 68382-546 | 68382-546-16 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-546-16) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | 7MG | ||||
| Approval Date: | Aug 3, 2017 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | 14MG | ||||
| Approval Date: | Aug 3, 2017 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | 21MG | ||||
| Approval Date: | Aug 3, 2017 | TE: | AB | RLD: | No | ||||
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