Thioridazine Hydrochloride
NDC 0378-0618, thioridazine hydrochloride, tablet, film coated, from Mylan Pharmaceuticals Inc..
- Product NDC
- 0378-0618
- Status
- Listed
- Labeler
- Mylan Pharmaceuticals Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA088004
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0378-0618 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- THIORIDAZINE HYDROCHLORIDE100 mg/1
Pharmacologic classes
Phenothiazine [EPC]; Phenothiazines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0378-0618-01 | 00378061801 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0618-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/56b3f4c2-52af-4947-b225-6808ae9f26f5NADAC price for package 00378061801
GET /v1/drugs/nadac/00378061801
Use it
Look up 0378-0618 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0378-0618 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0378-0618. 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.