| NDC Code | 57664-047-88 |
|---|
| Package Description | 100 CAPSULE in 1 BOTTLE (57664-047-88) |
|---|
| Product NDC | 57664-047 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Lisdexamfetamine Dimesylate |
|---|
| Non-Proprietary Name | Lisdexamfetamine Dimesylate |
|---|
| Dosage Form | CAPSULE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20230825 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA214484 |
|---|
| Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|
| Substance Name | LISDEXAMFETAMINE DIMESYLATE |
|---|
| Strength | 20 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE] |
|---|
| DEA Schedule | CII |
|---|