Depacon

Product NDC
0074-1564
11-digit product format
000741564
Labeler code
0074
Product ID
0074-1564_ccf25f30-b48d-88d0-49a4-1ed1f203d271
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Valproate Sodium
Dosage form
INJECTION
Route
INTRAVENOUS
Labeler
AbbVie Inc.
Application
NDA020593
Marketing category
NDA
Marketing start
1996-12-30
Marketing end
2019-11-01
Substance
VALPROATE SODIUM
Active strength
100 mg/mL
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0074-1564-10ML - Milliliter0074-15644de974da-0c8e-4811-8b58-9c4eeca317e212012-07-24