| NDC Code | 53489-150-10 |
|---|
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-150-10) |
|---|
| Product NDC | 53489-150 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Thioridazine Hydrochloride |
|---|
| Non-Proprietary Name | Thioridazine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19881007 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA089953 |
|---|
| Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|
| Substance Name | THIORIDAZINE HYDROCHLORIDE |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |
|---|