SUFLAVE
NDC 52268-550, polyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution, kit, from Braintree Laboratories, Inc..
- Product NDC
- 52268-550
- Status
- Listed
- Labeler
- Braintree Laboratories, Inc.
- Dosage form
- KIT
- Route
- —
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA215344
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/52268-550 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
None listed.
| Package NDC | NDC-11 | Package |
|---|---|---|
| 52268-550-01 | 52268055001 | 1 KIT in 1 KIT (52268-550-01) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/546cfc44-791c-4524-99a9-6a0af96c4ec8NADAC price for package 52268055001
GET /v1/drugs/nadac/52268055001
Use it
Look up 52268-550 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/52268-550 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 52268-550. 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.