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BROMSITE 0.075%

NDC 49708-754, bromfenac, solution/ drops, from Sun Pharmaceutical Industries, Inc..

Product NDC
49708-754
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA206911
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/49708-754 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BROMFENAC SODIUM.76 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
49708-754-41497080754411 POUCH in 1 CARTON (49708-754-41) / 1 BOTTLE, DROPPER in 1 POUCH / 5 mL in 1 BOTTLE, DROPPER

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/144a5072-341b-4591-8705-773b63044bcc

  • NADAC price for package 49708075441

    GET /v1/drugs/nadac/49708075441

Use it

Look up 49708-754 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/49708-754 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 49708-754. 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.