Thioridazine Hydrochloride 53489-0150
Product NDC
53489-0150- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 7, 1988
- Listing Expires
- December 31, 2026
- Application
- ANDA089953
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Thioridazine Hydrochloride | 50 mg/1 |
Drug Class
Phenothiazine [EPC]Phenothiazines [CS]
Packaging Options(2)
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-150-01)
1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-150-10)