Details for New Drug Application (NDA): 203175
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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. Two suppliers are listed for this compound. Additional details are available on the donepezil hydrochloride; memantine hydrochloride profile page.
Summary for 203175
Tradename: | MEMANTINE HYDROCHLORIDE |
Applicant: | Aurobindo Pharma Ltd |
Ingredient: | memantine hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 203175
Mechanism of Action | NMDA Receptor Antagonists |
Medical Subject Heading (MeSH) Categories for 203175
Suppliers and Packaging for NDA: 203175
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
MEMANTINE HYDROCHLORIDE | memantine hydrochloride | TABLET;ORAL | 203175 | ANDA | Aurobindo Pharma Limited | 65862-652 | 65862-652-03 | 3 BLISTER PACK in 1 CARTON (65862-652-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-652-10) |
MEMANTINE HYDROCHLORIDE | memantine hydrochloride | TABLET;ORAL | 203175 | ANDA | Aurobindo Pharma Limited | 65862-652 | 65862-652-60 | 60 TABLET, FILM COATED in 1 BOTTLE (65862-652-60) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 5MG | ||||
Approval Date: | Oct 13, 2015 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
Approval Date: | Oct 13, 2015 | TE: | AB | RLD: | No |
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