Valproic Acid

Product NDC

0603-1841

11-digit product format

006031841

Labeler code

0603

Product ID

0603-1841_49e1b0da-44f1-471d-bbe5-ed7d1c8ee016

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Valproic Acid

Dosage form

SOLUTION

Route

ORAL

Labeler

Par Pharmaceutical

Application

ANDA077960

Marketing category

ANDA

Marketing start

2006-10-13

Marketing end

2019-08-31

Substance

VALPROIC ACID

Active strength

250 mg/5mL

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record