SODIUM CHLORIDE
NDC 0338-9661, sodium chloride, injection, solution, from Baxter Healthcare Corporation.
- Product NDC
- 0338-9661
- Status
- Listed
- Labeler
- Baxter Healthcare Corporation
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA016677
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0338-9661 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM CHLORIDE9 g/1000mL
Pharmacologic classes
Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0338-9661-60 | 00338966160 | 100 mL in 1 BAG (0338-9661-60) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/958d35f0-6834-43be-a700-fa58f38b4c19
Use it
Look up 0338-9661 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0338-9661 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0338-9661. 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.