Dronabinol

Product NDC
0591-3593
11-digit product format
005913593
Labeler code
0591
Product ID
0591-3593_215cd577-6ad9-9a57-b91c-eee6958fe670
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Dronabinol
Dosage form
CAPSULE
Route
ORAL
Labeler
Actavis Pharma, Inc.
Application
NDA018651
Marketing category
NDA
Marketing start
1994-08-11
Marketing end
2019-09-30
Substance
DRONABINOL
Active strength
10 mg/1
Pharmacologic classes
Cannabinoid [EPC],Cannabinoids [CS]
DEA schedule
CIII
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
0591-3593-60EA - Each0591-359356538dab-1f92-47b5-b437-7f684f1e39c412013-02-13