Primidone

Product NDC

0615-7936

11-digit product format

006157936

Labeler code

0615

Product ID

0615-7936_c416f698-f27e-4490-a1b9-9b2cf4075d0e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

primidone

Dosage form

TABLET

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA040586

Marketing category

ANDA

Marketing start

2005-02-24

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record