Dronabinol

Product NDC

0591-3591

11-digit product format

005913591

Labeler code

0591

Product ID

0591-3591_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

2019-05-31

Substance

DRONABINOL

Active strength

3 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