| NDC Code | 0093-0811-01 |
|---|
| Package Description | 100 CAPSULE in 1 BOTTLE (0093-0811-01) |
|---|
| Product NDC | 0093-0811 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Nortriptyline Hydrochloride |
|---|
| Non-Proprietary Name | Nortriptyline Hydrochloride |
|---|
| Dosage Form | CAPSULE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19950406 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA074132 |
|---|
| Manufacturer | Teva Pharmaceuticals USA, Inc. |
|---|
| Substance Name | NORTRIPTYLINE HYDROCHLORIDE |
|---|
| Strength | 25 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Tricyclic Antidepressant [EPC] |
|---|