Dronabinol

Product NDC

68084-175

11-digit product format

680840175

Labeler code

68084

Product ID

68084-175_7df3366d-aedc-9352-e053-2991aa0a8cab

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Dronabinol

Dosage form

CAPSULE

Route

ORAL

Labeler

American Health Packaging

Application

ANDA078292

Marketing category

ANDA

Marketing start

2010-09-23

Marketing end

2019-10-31

Substance

DRONABINOL

Active strength

5 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