Primidone

Product NDC

0143-1482

11-digit product format

001431482

Labeler code

0143

Product ID

0143-1482_7d2a9a3b-a440-422e-afa1-7a4d41c2226a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Primidone

Dosage form

TABLET

Route

ORAL

Labeler

West-ward Pharmaceutical Corp

Application

ANDA040667

Marketing category

ANDA

Marketing start

2006-07-01

Marketing end

0000-00-00

Substance

PRIMIDONE

Active strength

50 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record