Details for New Drug Application (NDA): 022544
The generic ingredient in GRALISE is gabapentin. There is one drug master file entry for this compound. Ninety suppliers are listed for this compound. Additional details are available on the gabapentin profile page.
Summary for 022544
| Tradename: | GRALISE |
| Applicant: | Almatica |
| Ingredient: | gabapentin |
| Patents: | 0 |
Pharmacology for NDA: 022544
| Physiological Effect | Decreased Central Nervous System Disorganized Electrical Activity |
Suppliers and Packaging for NDA: 022544
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| GRALISE | gabapentin | TABLET;ORAL | 022544 | NDA | Almatica Pharma LLC | 52427-803 | 52427-803-90 | 90 TABLET, FILM COATED in 1 BOTTLE (52427-803-90) |
| GRALISE | gabapentin | TABLET;ORAL | 022544 | NDA | Almatica Pharma LLC | 52427-804 | 52427-804-60 | 60 TABLET, FILM COATED in 1 BOTTLE (52427-804-60) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 300MG | ||||
| Approval Date: | Jan 28, 2011 | TE: | AB2 | RLD: | Yes | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 600MG | ||||
| Approval Date: | Jan 28, 2011 | TE: | AB2 | RLD: | Yes | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 450MG | ||||
| Approval Date: | Apr 18, 2023 | TE: | AB | RLD: | Yes | ||||
Expired US Patents for NDA 022544
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Patent No. | Patent Expiration |
|---|---|---|---|---|---|---|---|
| Almatica | GRALISE | gabapentin | TABLET;ORAL | 022544-001 | Jan 28, 2011 | ⤷ Start Trial | ⤷ Start Trial |
| Almatica | GRALISE | gabapentin | TABLET;ORAL | 022544-001 | Jan 28, 2011 | ⤷ Start Trial | ⤷ Start Trial |
| Almatica | GRALISE | gabapentin | TABLET;ORAL | 022544-001 | Jan 28, 2011 | ⤷ Start Trial | ⤷ Start Trial |
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >Patent No. | >Patent Expiration |
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