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FENOPROFEN CALCIUM

NDC 16571-886, FENOPROFEN CALCIUM, capsule, from Rising Pharma Holdings, Inc..

Product NDC
16571-886
Status
Listed
Labeler
Rising Pharma Holdings, Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214475
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16571-886 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOPROFEN CALCIUM200 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
16571-886-0116571088601100 CAPSULE in 1 BOTTLE (16571-886-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4aa38cca-9f8f-4ab6-8103-4f1f48801a43

Use it

Look up 16571-886 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16571-886 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16571-886. 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.