Extended Phenytoin Sodium

Product NDC

50090-3142

11-digit product format

500903142

Labeler code

50090

Product ID

50090-3142_0e38fe70-d27c-474f-aeee-e3edd58a9f6c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Phenytoin Sodium

Dosage form

CAPSULE

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA204309

Marketing category

ANDA

Marketing start

2015-06-10

Marketing end

0000-00-00

Substance

PHENYTOIN SODIUM

Active strength

100 mg/1

Pharmacologic classes

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]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record