| NDC Code | 55700-619-30 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (55700-619-30) |
|---|
| Product NDC | 55700-619 |
|---|
| 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 | 20180511 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA202446 |
|---|
| Manufacturer | Lake Erie Medical DBA Quality Care Products LLC |
|---|
| Substance Name | AMITRIPTYLINE HYDROCHLORIDE |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Tricyclic Antidepressant [EPC] |
|---|