Details for New Drug Application (NDA): 078106
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The generic ingredient in LEVETIRACETAM is levetiracetam. There are thirty-five drug master file entries for this compound. Eighty-six suppliers are listed for this compound. Additional details are available on the levetiracetam profile page.
Summary for 078106
Tradename: | LEVETIRACETAM |
Applicant: | Prinston Inc |
Ingredient: | levetiracetam |
Patents: | 0 |
Pharmacology for NDA: 078106
Physiological Effect | Decreased Central Nervous System Disorganized Electrical Activity |
Suppliers and Packaging for NDA: 078106
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
LEVETIRACETAM | levetiracetam | TABLET;ORAL | 078106 | ANDA | Solco Healthcare US, LLC | 43547-221 | 43547-221-15 | 120 TABLET, FILM COATED in 1 BOTTLE (43547-221-15) |
LEVETIRACETAM | levetiracetam | TABLET;ORAL | 078106 | ANDA | Solco Healthcare US, LLC | 43547-222 | 43547-222-11 | 1000 TABLET, FILM COATED in 1 BOTTLE (43547-222-11) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 250MG | ||||
Approval Date: | Feb 10, 2009 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 500MG | ||||
Approval Date: | Feb 10, 2009 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 750MG | ||||
Approval Date: | Feb 10, 2009 | TE: | AB | RLD: | No |
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