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NDC 47335-507, cyclosporine, solution/ drops, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-507
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC, TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA210913
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-507 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CYCLOSPORINE.0009 mg/mL

Pharmacologic classes

Calcineurin Inhibitor Immunosuppressant [EPC]; Calcineurin Inhibitors [MoA]; Cytochrome P450 3A4 Inhibitors [MoA]; P-Glycoprotein Inhibitors [MoA]

Package NDCNDC-11Package
47335-507-97473350507971 POUCH in 1 BOX (47335-507-97) / 10 VIAL, SINGLE-DOSE in 1 POUCH / .25 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/48c3d8a3-4289-4b52-9189-58b48596095c

Use it

Look up 47335-507 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-507 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-507. 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.