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Vyvanse
Vyvanse - 35356-751-90 - (lisdexamfetamine dimesylate)
Drug Information of Vyvanse
| Product NDC: | 35356-751 |
| Proprietary Name: | Vyvanse |
| Non Proprietary Name: | lisdexamfetamine dimesylate |
| Active Ingredient(s): | 20 mg/1 & nbsp; lisdexamfetamine dimesylate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vyvanse
| Product NDC: | 35356-751 |
| Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021977 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20071210 |
Package Information of Vyvanse
| Package NDC: | 35356-751-90 |
| Package Description: | 90 CAPSULE in 1 BOTTLE (35356-751-90) |
NDC Information of Vyvanse
| NDC Code | 35356-751-90 |
| Proprietary Name | Vyvanse |
| Package Description | 90 CAPSULE in 1 BOTTLE (35356-751-90) |
| Product NDC | 35356-751 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | lisdexamfetamine dimesylate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20071210 |
| Marketing Category Name | NDA |
| Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
| Substance Name | LISDEXAMFETAMINE DIMESYLATE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |
