Potassium Chloride
NDC 50090-7378, Potassium Chloride, tablet, film coated, extended release, from A-S Medication Solutions.
- Product NDC
- 50090-7378
- Status
- Listed
- Labeler
- A-S Medication Solutions
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA209314
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7378 \ -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 |
|---|---|---|
| 50090-7378-0 | 50090737800 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7378-0) |
| 50090-7378-1 | 50090737801 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7378-1) |
| 50090-7378-2 | 50090737802 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7378-2) |
| 50090-7378-3 | 50090737803 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7378-3) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/0ac9b8dc-0c8e-4cdc-ab9d-bd8cab4f4958
Use it
Look up 50090-7378 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7378 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50090-7378. 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.