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Dronabinol
Dronabinol - 49884-869-05 - (Dronabinol)
Drug Information of Dronabinol
| Product NDC: | 49884-869 |
| Proprietary Name: | Dronabinol |
| 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 Dronabinol
| Product NDC: | 49884-869 |
| Labeler Name: | Par Pharmaceutical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078292 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080627 |
Package Information of Dronabinol
| Package NDC: | 49884-869-05 |
| Package Description: | 500 CAPSULE in 1 BOTTLE (49884-869-05) |
NDC Information of Dronabinol
| NDC Code | 49884-869-05 |
| Proprietary Name | Dronabinol |
| Package Description | 500 CAPSULE in 1 BOTTLE (49884-869-05) |
| Product NDC | 49884-869 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dronabinol |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20080627 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical Inc. |
| Substance Name | DRONABINOL |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cannabinoid [EPC],Cannabinoids [Chemical/Ingredient] |
