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Hydrocortisone Valerate

NDC 68462-836, HYDROCORTISONE VALERATE, ointment, from Glenmark Pharmaceuticals Inc., USA.

Product NDC
68462-836
Status
Listed
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
OINTMENT
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211750
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68462-836 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROCORTISONE VALERATE2 mg/g

Pharmacologic classes

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

Package NDCNDC-11Package
68462-836-17684620836171 TUBE in 1 CARTON (68462-836-17) / 15 g in 1 TUBE
68462-836-47684620836471 TUBE in 1 CARTON (68462-836-47) / 45 g in 1 TUBE
68462-836-65684620836651 TUBE in 1 CARTON (68462-836-65) / 60 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/18db91a0-fe67-4740-8a37-d656707356f1

Use it

Look up 68462-836 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68462-836 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68462-836. 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.