| NDC Code | 68788-9014-3 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (68788-9014-3) |
|---|
| Product NDC | 68788-9014 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Amitriptyline Hydrochloride |
|---|
| Non-Proprietary Name | Amitriptyline Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19771121 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA085966 |
|---|
| Manufacturer | Preferred Pharmaceuticals, Inc. |
|---|
| Substance Name | AMITRIPTYLINE HYDROCHLORIDE |
|---|
| Strength | 25 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Tricyclic Antidepressant [EPC] |
|---|