| NDC Code | 60760-907-90 |
|---|
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-907-90) |
|---|
| Product NDC | 60760-907 |
|---|
| 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 | 20210526 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA214548 |
|---|
| Manufacturer | ST. MARY'S MEDICAL PARK PHARMACY |
|---|
| Substance Name | AMITRIPTYLINE HYDROCHLORIDE |
|---|
| Strength | 100 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Tricyclic Antidepressant [EPC] |
|---|