Details for New Drug Application (NDA): 215069
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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 215069
Tradename: | LEVETIRACETAM |
Applicant: | Sciegen Pharms Inc |
Ingredient: | levetiracetam |
Patents: | 0 |
Pharmacology for NDA: 215069
Physiological Effect | Decreased Central Nervous System Disorganized Electrical Activity |
Suppliers and Packaging for NDA: 215069
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
LEVETIRACETAM | levetiracetam | TABLET;ORAL | 215069 | ANDA | A-S Medication Solutions | 50090-7333 | 50090-7333-1 | 60 TABLET, FILM COATED in 1 BOTTLE (50090-7333-1) |
LEVETIRACETAM | levetiracetam | TABLET;ORAL | 215069 | ANDA | A-S Medication Solutions | 50090-7333 | 50090-7333-2 | 180 TABLET, FILM COATED in 1 BOTTLE (50090-7333-2) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 750MG | ||||
Approval Date: | Jun 11, 2021 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 1GM | ||||
Approval Date: | Jun 11, 2021 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 250MG | ||||
Approval Date: | May 27, 2022 | TE: | AB | RLD: | No |
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