Details for New Drug Application (NDA): 090515
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The generic ingredient in LEVETIRACETAM is levetiracetam. There are thirty-five drug master file entries for this compound. Eighty-seven suppliers are listed for this compound. Additional details are available on the levetiracetam profile page.
Summary for 090515
Tradename: | LEVETIRACETAM |
Applicant: | Hetero Labs Ltd Iii |
Ingredient: | levetiracetam |
Patents: | 0 |
Pharmacology for NDA: 090515
Physiological Effect | Decreased Central Nervous System Disorganized Electrical Activity |
Suppliers and Packaging for NDA: 090515
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
LEVETIRACETAM | levetiracetam | TABLET;ORAL | 090515 | ANDA | NorthStar RxLLC | 16714-034 | 16714-034-01 | 120 TABLET, FILM COATED in 1 BOTTLE (16714-034-01) |
LEVETIRACETAM | levetiracetam | TABLET;ORAL | 090515 | ANDA | NorthStar RxLLC | 16714-034 | 16714-034-02 | 500 TABLET, FILM COATED in 1 BOTTLE (16714-034-02) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 250MG | ||||
Approval Date: | Oct 8, 2010 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 500MG | ||||
Approval Date: | Oct 8, 2010 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 750MG | ||||
Approval Date: | Oct 8, 2010 | TE: | AB | RLD: | No |
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