Phenytoin (Greenstone LLC)
Welcome to the PulseAid listing for the Phenytoin drug offered from Greenstone LLC. This Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Cytochrome P450 1A2 Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA],Cytochrome P450 2C8 Inducers [MoA],Cytochrome P450 2C19 Inducers [MoA],Cytochrome P450 2D6 Inducers [MoA],Cytochrome P450 3A Inducers [MoA],Cytochrome P450 2C9 Inducers [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: | Greenstone LLC |
NON-PROPRIETARY NAME: | Phenytoin |
SUBSTANCE NAME: | PHENYTOIN |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Cytochrome P450 1A2 Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA],Cytochrome P450 2C8 Inducers [MoA],Cytochrome P450 2C19 Inducers [MoA],Cytochrome P450 2D6 Inducers [MoA],Cytochrome P450 3A Inducers [MoA],Cytochrome P450 2C9 Inducers [MoA] |
ROUTE: | ORAL |
DOSAGE FORM: | SUSPENSION |
MARKETING CATEGORY NAME: | NDA AUTHORIZED GENERIC |
START MARKETING DATE: | 2012-10-09 |
END MARKETING DATE: | 0000-00-00 |
Phenytoin HUMAN PRESCRIPTION DRUG Details:
Item Description | Phenytoin from Greenstone LLC |
LABELER NAME: | Greenstone LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 125(mg/5mL) |
START MARKETING DATE: | 2012-10-09 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 59762-0531_67a0516a-ab81-4b74-9763-69ec3756aa2b |
PRODUCT NDC: | 59762-0531 |
APPLICATION NUMBER: | NDA008762 |
Other PHENYTOIN Pharmaceutical Manufacturers / Labelers: