Primidone - Primidone
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NDC Code: | 50268-687 |
Proprietary Name: | Primidone |
Suffix: | |
Non-Proprietary Name: | Primidone |
Dosage Form: | TABLET |
Method: | ORAL |
Original Marketing Date: | 19-05-2011 |
Category Name: | ANDA |
Application Number: | ANDA040866 |
Labeler: | AVPAK |
Substance Name: | PRIMIDONE |
Active Numerator Strength: | 250 |
Active Ingredient Unit: | mg/1 |
Pharm Classes: | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
DEA Schedule: |