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PRIMIDONE
PRIMIDONE - 42549-680-30 - (PRIMIDONE)
Drug Information of PRIMIDONE
| Product NDC: | 42549-680 |
| Proprietary Name: | PRIMIDONE |
| Non Proprietary Name: | PRIMIDONE |
| Active Ingredient(s): | 50 mg/1 & nbsp; PRIMIDONE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PRIMIDONE
| Product NDC: | 42549-680 |
| Labeler Name: | STAT Rx USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA084903 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010524 |
Package Information of PRIMIDONE
| Package NDC: | 42549-680-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (42549-680-30) |
NDC Information of PRIMIDONE
| NDC Code | 42549-680-30 |
| Proprietary Name | PRIMIDONE |
| Package Description | 30 TABLET in 1 BOTTLE (42549-680-30) |
| Product NDC | 42549-680 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PRIMIDONE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20010524 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT Rx USA LLC |
| Substance Name | PRIMIDONE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
