Thioridazine Hydrochloride
NDC 62135-938, Thioridazine Hydrochloride, tablet, film coated, from Chartwell RX, LLC.
- Product NDC
- 62135-938
- Status
- Listed
- Labeler
- Chartwell RX, LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA088134
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/62135-938 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- THIORIDAZINE HYDROCHLORIDE50 mg/1
Pharmacologic classes
Phenothiazine [EPC]; Phenothiazines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 62135-938-90 | 62135093890 | 90 TABLET, FILM COATED in 1 BOTTLE (62135-938-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/e0bbe982-6434-468b-bd29-64ac57386fbe
Use it
Look up 62135-938 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/62135-938 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 62135-938. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.