Potassium Citrate
NDC 72162-1758, Potassium Citrate, tablet, extended release, from Bryant Ranch Prepack.
- Product NDC
- 72162-1758
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA212779
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1758 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- POTASSIUM CITRATE10 meq/1
Pharmacologic classes
Acidifying Activity [MoA]; Anti-coagulant [EPC]; Calcium Chelating Activity [MoA]; Calculi Dissolution Agent [EPC]; Decreased Coagulation Factor Activity [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72162-1758-1 | 72162175801 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1758-1) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/595343aa-b760-4158-9c49-dd5368f45e2c
Use it
Look up 72162-1758 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1758 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72162-1758. 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.