Potassium Chloride
NDC 70518-4050, Potassium Chloride, capsule, extended release, from REMEDYREPACK INC..
- Product NDC
- 70518-4050
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA214686
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4050 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- POTASSIUM CHLORIDE750 mg/1
Pharmacologic classes
Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Potassium Compounds [CS]; Potassium Salt [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70518-4050-0 | 70518405000 | 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-4050-0) |
| 70518-4050-1 | 70518405001 | 100 POUCH in 1 BOX (70518-4050-1) / 1 CAPSULE, EXTENDED RELEASE in 1 POUCH (70518-4050-2) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/f75713cf-6902-4160-94cb-335a1ecdbbbe
Use it
Look up 70518-4050 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4050 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-4050. 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.