Primidone

Product NDC

50090-1636

11-digit product format

500901636

Labeler code

50090

Product ID

50090-1636_e569e679-bf6c-4947-ae8a-750a6415bf95

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Primidone

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA040866

Marketing category

ANDA

Marketing start

2009-12-24

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

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record