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Difluprednate

NDC 46708-750, difluprednate ophthalmic, emulsion, from Alembic Pharmaceuticals Limited.

Product NDC
46708-750
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
Dosage form
EMULSION
Route
OPHTHALMIC
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213774
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/46708-750 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIFLUPREDNATE.5 mg/mL
Package NDCNDC-11Package
46708-750-05467080750051 BOTTLE in 1 CARTON (46708-750-05) / 5 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/71121026-1496-4154-b61b-9afe9b62bf2a

Use it

Look up 46708-750 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-750 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-750. 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.