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Azelastine Hydrochloride

NDC 47335-938, Azelastine Hydrochloride, solution/ drops, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-938
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
SOLUTION/ DROPS
Route
INTRAOCULAR
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078738
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-938 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AZELASTINE HYDROCHLORIDE.5 mg/mL

Pharmacologic classes

Histamine H1 Receptor Antagonists [MoA]; Histamine-1 Receptor Antagonist [EPC]

Package NDCNDC-11Package
47335-938-90473350938901 BOTTLE, PLASTIC in 1 BOX (47335-938-90) / 6 mL in 1 BOTTLE, PLASTIC

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/04e5eede-17ff-4765-af77-d46c139da703

Use it

Look up 47335-938 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-938 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-938. 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.