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IBUPROFEN

NDC 68071-5135, IBUPROFEN, tablet, film coated, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-5135
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090796
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-5135 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • IBUPROFEN800 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68071-5135-068071513500100 TABLET, FILM COATED in 1 BOTTLE (68071-5135-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/99d7cf65-3ec2-24eb-e053-2a95a90acc5e

Use it

Look up 68071-5135 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-5135 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-5135. 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.