CHLORTHALIDONE
NDC 70518-3718, chlorthalidone, tablet, from REMEDYREPACK INC..
- Product NDC
- 70518-3718
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA215587
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3718 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CHLORTHALIDONE25 mg/1
Pharmacologic classes
Increased Diuresis [PE]; Thiazide-like Diuretic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70518-3718-0 | 70518371800 | 30 TABLET in 1 BLISTER PACK (70518-3718-0) |
| 70518-3718-1 | 70518371801 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-3718-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/0baac2aa-06c4-489e-a3f9-fe9d20cf61a2
Use it
Look up 70518-3718 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3718 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-3718. 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.