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Hydrocortisone sodium succinate

NDC 70710-1907, Hydrocortisone sodium succinate, injection, from Zydus Pharmaceuticals USA Inc..

Product NDC
70710-1907
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
INJECTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217191
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1907 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROCORTISONE SODIUM SUCCINATE100 mg/2mL

Pharmacologic classes

Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]

Package NDCNDC-11Package
70710-1907-1707101907011 VIAL in 1 CARTON (70710-1907-1) / 2 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/37534164-9de5-4bb3-9f87-341dfcf90883

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=70710-1907

  • NADAC price for package 70710190701

    GET /v1/drugs/nadac/70710190701

Use it

Look up 70710-1907 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1907 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1907. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.