| NDC Code | 68071-2931-3 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (68071-2931-3) |
|---|
| Product NDC | 68071-2931 |
|---|
| 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 | 20210825 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA210086 |
|---|
| Manufacturer | NuCare Pharmaceuticals,Inc. |
|---|
| Substance Name | AMITRIPTYLINE HYDROCHLORIDE |
|---|
| Strength | 25 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Tricyclic Antidepressant [EPC] |
|---|