Succinylcholine Chloride
NDC 70771-1352, Succinylcholine Chloride, injection, solution, from Zydus Lifesciences Limited.
- Product NDC
- 70771-1352
- Status
- Listed
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR, INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA209467
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1352 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SUCCINYLCHOLINE CHLORIDE20 mg/mL
Pharmacologic classes
Depolarizing Neuromuscular Blocker [EPC]; Neuromuscular Depolarizing Blockade [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70771-1352-7 | 70771135207 | 25 VIAL, MULTI-DOSE in 1 TRAY (70771-1352-7) / 10 mL in 1 VIAL, MULTI-DOSE (70771-1352-1) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/c7f409ed-e4f4-4cd6-8f37-93f505dd986d
Use it
Look up 70771-1352 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1352 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70771-1352. 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.