Chlorpromazine Hydrochloride
NDC 70518-3510, Chlorpromazine Hydrochloride, tablet, sugar coated, from REMEDYREPACK INC..
- Product NDC
- 70518-3510
- 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/70518-3510 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CHLORPROMAZINE HYDROCHLORIDE25 mg/1
Pharmacologic classes
Phenothiazine [EPC]; Phenothiazines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70518-3510-0 | 70518351000 | 30 TABLET, SUGAR COATED in 1 BLISTER PACK (70518-3510-0) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/2122d619-3f5b-48f6-8f0b-7693199abbdb
Use it
Look up 70518-3510 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3510 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-3510. 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.