dantrolene sodium
NDC 70518-4668, dantrolene sodium, capsule, from REMEDYREPACK INC..
- Product NDC
- 70518-4668
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- CAPSULE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA017443
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4668 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DANTROLENE SODIUM50 mg/1
Pharmacologic classes
Decreased Striated Muscle Contraction [PE]; Decreased Striated Muscle Tone [PE]; Skeletal Muscle Relaxant [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70518-4668-0 | 70518466800 | 50 POUCH in 1 BOX (70518-4668-0) / 1 CAPSULE in 1 POUCH (70518-4668-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/35f62a81-653f-4a3c-a797-d39304dcd08c
Use it
Look up 70518-4668 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4668 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-4668. 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.