Marinol - 0051-0023-21 - (Dronabinol)

Alphabetical Index


Drug Information of Marinol

Product NDC: 0051-0023
Proprietary Name: Marinol
Non Proprietary Name: Dronabinol
Active Ingredient(s): 10    mg/1 & nbsp;   Dronabinol
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Marinol

Product NDC: 0051-0023
Labeler Name: Abbott Products, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018651
Marketing Category: NDA
Start Marketing Date: 20100713

Package Information of Marinol

Package NDC: 0051-0023-21
Package Description: 60 CAPSULE in 1 BOTTLE (0051-0023-21)

NDC Information of Marinol

NDC Code 0051-0023-21
Proprietary Name Marinol
Package Description 60 CAPSULE in 1 BOTTLE (0051-0023-21)
Product NDC 0051-0023
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dronabinol
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100713
Marketing Category Name NDA
Labeler Name Abbott Products, Inc.
Substance Name DRONABINOL
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Cannabinoid [EPC],Cannabinoids [Chemical/Ingredient]

Complete Information of Marinol


General Information