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SULINDAC

NDC 71205-648, SULINDAC, tablet, from Proficient Rx LP.

Product NDC
71205-648
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA072711
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-648 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SULINDAC200 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71205-648-307120506483030 TABLET in 1 BOTTLE (71205-648-30)
71205-648-607120506486060 TABLET in 1 BOTTLE (71205-648-60)
71205-648-907120506489090 TABLET in 1 BOTTLE (71205-648-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d94e8865-d151-4fb1-bacd-f4e43819e3c2

Use it

Look up 71205-648 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-648 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-648. 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.