Valproic Acid

Product NDC
60432-621
11-digit product format
604320621
Labeler code
60432
Product ID
60432-621_734c46b6-3359-44a5-a4bc-b308f1970e23
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Valproic Acid
Dosage form
SOLUTION
Route
ORAL
Labeler
Morton Grove Pharmaceuticals, Inc.
Application
ANDA070868
Marketing category
ANDA
Marketing start
1986-07-01
Marketing end
0000-00-00
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
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60432-621-16ML - Milliliter60432-62112034c94-7ae3-4ca7-8194-3403bfcedd5112012-07-24

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60432-621VALPROIC ACID SOLUTION [MORTON GROVE PHARMACEUTICALS, INC.]16Legacy NDC20210124_7af84664-7e3b-43f3-a43e-beba36ffb739.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
60432-621-1660432062116473 mL in 1 BOTTLE, PLASTIC (60432-621-16) 473 ml1986-07-010000-00-00NoNoCurrent