E-Z-Paque
NDC 32909-750, barium sulfate, powder, for suspension, from E-Z-EM Canada Inc.
- Product NDC
- 32909-750
- Status
- Listed
- Labeler
- E-Z-EM Canada Inc
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA208036
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/32909-750 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BARIUM SULFATE960 mg/g
Pharmacologic classes
Radiographic Contrast Agent [EPC]; X-Ray Contrast Activity [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 32909-750-03 | 32909075003 | 24 BOTTLE, PLASTIC in 1 CARTON (32909-750-03) / 176 g in 1 BOTTLE, PLASTIC |
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/7225868a-4037-c96a-44e3-3326d36cbedc
Use it
Look up 32909-750 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/32909-750 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 32909-750. 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.