Primidone

Product NDC

0615-2521

11-digit product format

006152521

Labeler code

0615

Product ID

0615-2521_8757a56a-c01b-4d1d-93e1-3e18ec381daf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

primidone

Dosage form

TABLET

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA040667

Marketing category

ANDA

Marketing start

2006-07-01

Marketing end

0000-00-00

Substance

PRIMIDONE

Active strength

250 mg/1

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record