Details for New Drug Application (NDA): 075350
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The generic ingredient in GABAPENTIN is gabapentin. There are twenty-nine drug master file entries for this compound. Seventy-eight suppliers are listed for this compound. Additional details are available on the gabapentin profile page.
Summary for 075350
Tradename: | GABAPENTIN |
Applicant: | Actavis Elizabeth |
Ingredient: | gabapentin |
Patents: | 0 |
Pharmacology for NDA: 075350
Physiological Effect | Decreased Central Nervous System Disorganized Electrical Activity |
Suppliers and Packaging for NDA: 075350
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
GABAPENTIN | gabapentin | CAPSULE;ORAL | 075350 | ANDA | Aphena Pharma Solutions - Tennessee, LLC | 43353-075 | 43353-075-30 | 30 CAPSULE in 1 BOTTLE (43353-075-30) |
GABAPENTIN | gabapentin | CAPSULE;ORAL | 075350 | ANDA | Aphena Pharma Solutions - Tennessee, LLC | 43353-075 | 43353-075-60 | 90 CAPSULE in 1 BOTTLE (43353-075-60) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 100MG | ||||
Approval Date: | Sep 12, 2003 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 300MG | ||||
Approval Date: | Sep 12, 2003 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 400MG | ||||
Approval Date: | Sep 12, 2003 | TE: | AB | RLD: | No |
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