Dronabinol - 68084-174-01 - (Dronabinol)

Alphabetical Index


Drug Information of Dronabinol

Product NDC: 68084-174
Proprietary Name: Dronabinol
Non Proprietary Name: Dronabinol
Active Ingredient(s): 2.5    mg/1 & nbsp;   Dronabinol
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Dronabinol

Product NDC: 68084-174
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078292
Marketing Category: ANDA
Start Marketing Date: 20100907

Package Information of Dronabinol

Package NDC: 68084-174-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-174-01) > 10 CAPSULE in 1 BLISTER PACK (68084-174-11)

NDC Information of Dronabinol

NDC Code 68084-174-01
Proprietary Name Dronabinol
Package Description 10 BLISTER PACK in 1 CARTON (68084-174-01) > 10 CAPSULE in 1 BLISTER PACK (68084-174-11)
Product NDC 68084-174
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dronabinol
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100907
Marketing Category Name ANDA
Labeler Name American Health Packaging
Substance Name DRONABINOL
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Cannabinoid [EPC],Cannabinoids [Chemical/Ingredient]

Complete Information of Dronabinol


General Information