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Gralise
Gralise - 13913-006-16 - (gabapentin)
Drug Information of Gralise
| Product NDC: | 13913-006 |
| Proprietary Name: | Gralise |
| Non Proprietary Name: | gabapentin |
| Active Ingredient(s): | & nbsp; gabapentin |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Gralise
| Product NDC: | 13913-006 |
| Labeler Name: | Depomed, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022544 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110128 |
Package Information of Gralise
| Package NDC: | 13913-006-16 |
| Package Description: | 1 KIT in 1 BLISTER PACK (13913-006-16) |
NDC Information of Gralise
| NDC Code | 13913-006-16 |
| Proprietary Name | Gralise |
| Package Description | 1 KIT in 1 BLISTER PACK (13913-006-16) |
| Product NDC | 13913-006 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | gabapentin |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20110128 |
| Marketing Category Name | NDA |
| Labeler Name | Depomed, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
