| NDC Code | 68788-7552-1 |
|---|
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7552-1) |
|---|
| Product NDC | 68788-7552 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Desipramine Hydrochloride |
|---|
| Non-Proprietary Name | Desipramine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20190122 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA205153 |
|---|
| Manufacturer | Preferred Pharmaceuticals, Inc. |
|---|
| Substance Name | DESIPRAMINE HYDROCHLORIDE |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Tricyclic Antidepressant [EPC] |
|---|