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Flunisolide

NDC 68682-344, Flunisolide, solution, from Oceanside Pharmaceuticals.

Product NDC
68682-344
Status
Listed
Labeler
Oceanside Pharmaceuticals
Dosage form
SOLUTION
Route
NASAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074805
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68682-344 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLUNISOLIDE.25 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
68682-344-25686820344251 BOTTLE, PUMP in 1 CARTON (68682-344-25) / 25 mL in 1 BOTTLE, PUMP

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/50d87523-e1fb-4342-825f-9dba972c6a25

Use it

Look up 68682-344 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68682-344 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68682-344. 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.