Sodium Citrate and Citric Acid
NDC 50268-182, SODIUM CITRATE and CITRIC ACID MONOHYDRATE, solution, from AvPAK.
- Product NDC
- 50268-182
- Status
- Listed
- Labeler
- AvPAK
- Dosage form
- SOLUTION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50268-182 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM CITRATE500 mg/5mL
- ANHYDROUS CITRIC ACID334 mg/5mL
Pharmacologic classes
Acidifying Activity [MoA]; Acidifying Activity [MoA]; Anti-coagulant [EPC]; Anti-coagulant [EPC]; Calcium Chelating Activity [MoA]; Calcium Chelating Activity [MoA]; Calculi Dissolution Agent [EPC]; Calculi Dissolution Agent [EPC]; Decreased Coagulation Factor Activity [PE]; Decreased Coagulation Factor Activity [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 50268-182-15 | 50268018215 | 40 CUP, UNIT-DOSE in 1 CARTON (50268-182-15) / 15 mL in 1 CUP, UNIT-DOSE (50268-182-11) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/fe070e2e-3e72-fb84-e053-6294a90afd88
Use it
Look up 50268-182 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50268-182 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50268-182. 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.