| NDC Code | 53002-4910-3 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (53002-4910-3) |
|---|
| Product NDC | 53002-4910 |
|---|
| 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 | 20141205 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA202446 |
|---|
| Manufacturer | RPK Pharmaceuticals, Inc. |
|---|
| Substance Name | AMITRIPTYLINE HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Tricyclic Antidepressant [EPC] |
|---|