| NDC Code | 29300-420-10 |
|---|
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (29300-420-10) |
|---|
| Product NDC | 29300-420 |
|---|
| 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 | Unichem Pharmaceuticals (USA), Inc. |
|---|
| Substance Name | AMITRIPTYLINE HYDROCHLORIDE |
|---|
| Strength | 25 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Tricyclic Antidepressant [EPC] |
|---|