Depakene

Product NDC
0074-5681
11-digit product format
000745681
Labeler code
0074
Product ID
0074-5681_50cd723a-f8b9-0c3f-e4c7-bf761f535552
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Valproic Acid
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
AbbVie Inc.
Application
NDA018081
Marketing category
NDA
Marketing start
1978-02-28
Marketing end
2019-10-11
Substance
VALPROIC ACID
Active strength
250 mg/1
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
0074-5681-13EA - Each0074-568146a817d4-d4b3-4439-b866-0eba964880f512012-07-24