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Dronabinol
Dronabinol - 0378-8170-91 - (Dronabinol)
Drug Information of Dronabinol
| Product NDC: | 0378-8170 |
| Proprietary Name: | Dronabinol |
| Non Proprietary Name: | Dronabinol |
| Active Ingredient(s): | 2.5 mg/1 & nbsp; Dronabinol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dronabinol
| Product NDC: | 0378-8170 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078501 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111101 |
Package Information of Dronabinol
| Package NDC: | 0378-8170-91 |
| Package Description: | 60 CAPSULE, LIQUID FILLED in 1 BOTTLE, UNIT-DOSE (0378-8170-91) |
NDC Information of Dronabinol
| NDC Code | 0378-8170-91 |
| Proprietary Name | Dronabinol |
| Package Description | 60 CAPSULE, LIQUID FILLED in 1 BOTTLE, UNIT-DOSE (0378-8170-91) |
| Product NDC | 0378-8170 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dronabinol |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20111101 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | DRONABINOL |
| Strength Number | 2.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cannabinoid [EPC],Cannabinoids [Chemical/Ingredient] |
