LumaSon
NDC 0270-7097, SULFUR HEXAFLUORIDE, injection, powder, lyophilized, for suspension, from BRACCO DIAGNOSTICS INC.
- Product NDC
- 0270-7097
- Status
- Listed
- Labeler
- BRACCO DIAGNOSTICS INC
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION
- Route
- INTRAVENOUS, INTRAVESICAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA203684
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0270-7097 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SULFUR HEXAFLUORIDE60.7 mg/mg
- DISTEAROYLPHOSPHATIDYLCHOLINE, DL-.19 mg/mg
- SODIUM 1,2-DIPALMITOYL-SN-GLYCERO-3-PHOSPHO-(1'-RAC-GLYCEROL).19 mg/mg
Pharmacologic classes
Contrast Agent for Ultrasound Imaging [EPC]; Ultrasound Contrast Activity [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0270-7097-07 | 00270709707 | 20 VIAL in 1 BOX (0270-7097-07) / 25 mg in 1 VIAL |
| 0270-7097-08 | 00270709708 | 20 VIAL in 1 BOX (0270-7097-08) / 25 mg in 1 VIAL |
Linked data
RxNorm, label and prices
RxNorm concepts
RxNorm links no concept to this product's packages.
Related lookups
FDA label sections
GET /v1/drugs/labels?ndc=0270-7097Medicare Part B payment limits (ASP)
GET /v1/drugs/asp?ndc=0270-7097
Use it
Look up 0270-7097 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0270-7097 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0270-7097. 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.