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Neurontin
Neurontin - 52125-077-02 - (gabapentin)
Drug Information of Neurontin
| Product NDC: | 52125-077 |
| Proprietary Name: | Neurontin |
| Non Proprietary Name: | gabapentin |
| Active Ingredient(s): | 300 mg/1 & nbsp; gabapentin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Neurontin
| Product NDC: | 52125-077 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020235 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120917 |
Package Information of Neurontin
| Package NDC: | 52125-077-02 |
| Package Description: | 30 CAPSULE in 1 BLISTER PACK (52125-077-02) |
NDC Information of Neurontin
| NDC Code | 52125-077-02 |
| Proprietary Name | Neurontin |
| Package Description | 30 CAPSULE in 1 BLISTER PACK (52125-077-02) |
| Product NDC | 52125-077 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | gabapentin |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20120917 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | GABAPENTIN |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
