| NDC Code | 69367-389-01 |
|---|
| Package Description | 100 TABLET, COATED in 1 BOTTLE (69367-389-01) |
|---|
| Product NDC | 69367-389 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Amitriptyline Hydrochloride |
|---|
| Non-Proprietary Name | Amitriptyline Hydrochloride |
|---|
| Dosage Form | TABLET, COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20240520 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA212654 |
|---|
| Manufacturer | Westminster Pharmaceuticals, LLC |
|---|
| Substance Name | AMITRIPTYLINE HYDROCHLORIDE |
|---|
| Strength | 25 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Tricyclic Antidepressant [EPC] |
|---|