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Marinol
Marinol - 0051-0022-21 - (Dronabinol)
Drug Information of Marinol
| Product NDC: | 0051-0022 |
| Proprietary Name: | Marinol |
| Non Proprietary Name: | Dronabinol |
| Active Ingredient(s): | 5 mg/1 & nbsp; Dronabinol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Marinol
| Product NDC: | 0051-0022 |
| 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: | 0051-0022-21 |
| Package Description: | 60 CAPSULE in 1 BOTTLE (0051-0022-21) |
NDC Information of Marinol
| NDC Code | 0051-0022-21 |
| Proprietary Name | Marinol |
| Package Description | 60 CAPSULE in 1 BOTTLE (0051-0022-21) |
| Product NDC | 0051-0022 |
| 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 | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cannabinoid [EPC],Cannabinoids [Chemical/Ingredient] |
