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Gabapentin
Gabapentin - 49349-898-02 - (Gabapentin)
Drug Information of Gabapentin
| Product NDC: | 49349-898 |
| Proprietary Name: | Gabapentin |
| Non Proprietary Name: | Gabapentin |
| Active Ingredient(s): | 600 mg/1 & nbsp; Gabapentin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Gabapentin
| Product NDC: | 49349-898 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200651 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120307 |
Package Information of Gabapentin
| Package NDC: | 49349-898-02 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (49349-898-02) |
NDC Information of Gabapentin
| NDC Code | 49349-898-02 |
| Proprietary Name | Gabapentin |
| Package Description | 30 TABLET in 1 BLISTER PACK (49349-898-02) |
| Product NDC | 49349-898 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Gabapentin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120307 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | GABAPENTIN |
| Strength Number | 600 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
