Potassium Chloride
NDC 70518-2964, Potassium Chloride, tablet, film coated, extended release, from REMEDYREPACK INC..
- Product NDC
- 70518-2964
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210921
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2964 \ -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 |
|---|---|---|
| 70518-2964-0 | 70518296400 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-2964-0) |
| 70518-2964-3 | 70518296403 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2964-3) |
| 70518-2964-4 | 70518296404 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2964-4) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/16c775e4-0dd8-4e9f-b2bf-dd2b639374cf
Use it
Look up 70518-2964 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2964 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-2964. 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.