| NDC Code | 58118-2212-6 |
|---|
| Package Description | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58118-2212-6) |
|---|
| Product NDC | 58118-2212 |
|---|
| 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 | 19970911 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040218 |
|---|
| Manufacturer | Clinical Solutions Wholesale |
|---|
| Substance Name | AMITRIPTYLINE HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Tricyclic Antidepressant [EPC] |
|---|