Details for New Drug Application (NDA): 208672
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The generic ingredient in MEMANTINE HYDROCHLORIDE AND DONEPEZIL 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 208672
| Tradename: | MEMANTINE HYDROCHLORIDE AND DONEPEZIL HYDROCHLORIDE |
| Applicant: | Macleods Pharms Ltd |
| Ingredient: | donepezil hydrochloride; memantine hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 208672
| Mechanism of Action | Cholinesterase Inhibitors NMDA Receptor Antagonists |
Suppliers and Packaging for NDA: 208672
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| MEMANTINE HYDROCHLORIDE AND DONEPEZIL HYDROCHLORIDE | donepezil hydrochloride; memantine hydrochloride | CAPSULE, EXTENDED RELEASE;ORAL | 208672 | ANDA | Macleods Pharmaceuticals Limited | 33342-312 | 33342-312-07 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-312-07) |
| MEMANTINE HYDROCHLORIDE AND DONEPEZIL HYDROCHLORIDE | donepezil hydrochloride; memantine hydrochloride | CAPSULE, EXTENDED RELEASE;ORAL | 208672 | ANDA | Macleods Pharmaceuticals Limited | 33342-312 | 33342-312-10 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-312-10) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | 10MG;14MG | ||||
| Approval Date: | Jul 15, 2025 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | 10MG;28MG | ||||
| Approval Date: | Jul 15, 2025 | TE: | AB | RLD: | No | ||||
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