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Tolectin

NDC 50991-988, tolmetin sodium, tablet, film coated, from Poly Pharmaceuticals, Inc..

Product NDC
50991-988
Status
Listed
Labeler
Poly Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074473
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50991-988 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TOLMETIN SODIUM600 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
50991-988-305099109883030 TABLET, FILM COATED in 1 BOTTLE (50991-988-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/15467b19-e43a-5be9-e063-6294a90a3cca

Use it

Look up 50991-988 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50991-988 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50991-988. 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.