Potassium Chloride
NDC 71610-349, Potassium Chloride, tablet, film coated, extended release, from Aphena Pharma Solutions - Tennessee, LLC.
- Product NDC
- 71610-349
- Status
- Listed
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA019123
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71610-349 \ -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 |
|---|---|---|
| 71610-349-15 | 71610034915 | 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-15) |
| 71610-349-30 | 71610034930 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-30) |
| 71610-349-45 | 71610034945 | 45 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-45) |
| 71610-349-53 | 71610034953 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-53) |
| 71610-349-60 | 71610034960 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-60) |
| 71610-349-70 | 71610034970 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-70) |
| 71610-349-80 | 71610034980 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-80) |
| 71610-349-85 | 71610034985 | 200 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-85) |
| 71610-349-92 | 71610034992 | 270 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-92) |
| 71610-349-94 | 71610034994 | 360 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-94) |
| 71610-349-98 | 71610034998 | 540 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-98) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/81a53ecd-2612-4efe-9491-415fff3f86e5
Use it
Look up 71610-349 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71610-349 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71610-349. 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.