Chlorpromazine Hydrochloride
NDC 70518-3584, Chlorpromazine Hydrochloride, tablet, sugar coated, from REMEDYREPACK INC..
- Product NDC
- 70518-3584
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA214827
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3584 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CHLORPROMAZINE HYDROCHLORIDE100 mg/1
Pharmacologic classes
Phenothiazine [EPC]; Phenothiazines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70518-3584-1 | 70518358401 | 100 POUCH in 1 BOX (70518-3584-1) / 1 TABLET, SUGAR COATED in 1 POUCH (70518-3584-2) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/d3b09b67-e8da-450d-8a52-b3c40605de26
Use it
Look up 70518-3584 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3584 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-3584. 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.