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Flurbiprofen Sodium

NDC 24208-314, Flurbiprofen Sodium, solution/ drops, from Bausch & Lomb Incorporated.

Product NDC
24208-314
Status
Listed
Labeler
Bausch & Lomb Incorporated
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074447
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/24208-314 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLURBIPROFEN SODIUM.3 mg/mL

Pharmacologic classes

Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Nonsteroidal Anti-inflammatory Drug [EPC]

Package NDCNDC-11Package
24208-314-25242080314251 BOTTLE, DROPPER in 1 CARTON (24208-314-25) / 2.5 mL in 1 BOTTLE, DROPPER

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/11db354f-caf9-4567-811e-6c9beb1330c7

Use it

Look up 24208-314 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/24208-314 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 24208-314. 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.