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DIFLUPREDNATE

NDC 69097-341, DIFLUPREDNATE, emulsion, from Cipla USA Inc..

Product NDC
69097-341
Status
Listed
Labeler
Cipla USA Inc.
Dosage form
EMULSION
Route
OPHTHALMIC
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211776
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69097-341 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIFLUPREDNATE.5 mg/mL
Package NDCNDC-11Package
69097-341-35690970341351 BOTTLE in 1 CARTON (69097-341-35) / 5 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8a7254de-a7a2-476d-9295-c41926267ec9

Use it

Look up 69097-341 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69097-341 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69097-341. 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.