| NDC Code | 72989-409-11 |
|---|
| Package Description | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72989-409-11) |
|---|
| Product NDC | 72989-409 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Phendimetrazine Tartrate |
|---|
| Non-Proprietary Name | Phendimetrazine Tartrate |
|---|
| Dosage Form | CAPSULE, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20221101 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA018074 |
|---|
| Manufacturer | Acertis Pharmaceuticals, LLC |
|---|
| Substance Name | PHENDIMETRAZINE TARTRATE |
|---|
| Strength | 105 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Appetite Suppression [PE], Increased Sympathetic Activity [PE], Sympathomimetic Amine Anorectic [EPC] |
|---|
| DEA Schedule | CIII |
|---|