NDC 53489-150
Thioridazine Hydrochloride
Thioridazine Hydrochloride
Thioridazine Hydrochloride is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is Thioridazine Hydrochloride.
Product ID | 53489-150_2c96c6f9-3008-48ba-86ea-e9b83502da67 |
NDC | 53489-150 |
Product Type | Human Prescription Drug |
Proprietary Name | Thioridazine Hydrochloride |
Generic Name | Thioridazine Hydrochloride |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 1988-10-07 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA089953 |
Labeler Name | Sun Pharmaceutical Industries, Inc. |
Substance Name | THIORIDAZINE HYDROCHLORIDE |
Active Ingredient Strength | 50 mg/1 |
Pharm Classes | Phenothiazine [EPC],Phenothiazines [CS] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |