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Primidone
Primidone - 0115-1031-03 - (PRIMIDONE)
Drug Information of Primidone
| Product NDC: | 0115-1031 |
| Proprietary Name: | Primidone |
| Non Proprietary Name: | PRIMIDONE |
| Active Ingredient(s): | 250 mg/1 & nbsp; PRIMIDONE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Primidone
| Product NDC: | 0115-1031 |
| Labeler Name: | Global Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040717 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080212 |
Package Information of Primidone
| Package NDC: | 0115-1031-03 |
| Package Description: | 1000 TABLET in 1 BOTTLE (0115-1031-03) |
NDC Information of Primidone
| NDC Code | 0115-1031-03 |
| Proprietary Name | Primidone |
| Package Description | 1000 TABLET in 1 BOTTLE (0115-1031-03) |
| Product NDC | 0115-1031 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PRIMIDONE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20080212 |
| Marketing Category Name | ANDA |
| Labeler Name | Global Pharmaceuticals |
| Substance Name | PRIMIDONE |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
