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Diclofenac Sodium and Misoprostol

NDC 42291-232, Diclofenac Sodium and Misoprostol, tablet, delayed release, from AvKARE.

Product NDC
42291-232
Status
Listed
Labeler
AvKARE
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA201089
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42291-232 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DICLOFENAC SODIUM50 mg/1
  • MISOPROSTOL200 ug/1

Pharmacologic classes

Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Decreased Prostaglandin Production [PE]; Nonsteroidal Anti-inflammatory Drug [EPC]; Prostaglandin E1 Analog [EPC]; Prostaglandins E, Synthetic [CS]

Package NDCNDC-11Package
42291-232-604229102326060 TABLET, DELAYED RELEASE in 1 BOTTLE (42291-232-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3643ab1b-9f8f-b2f4-e02d-950d0a02e587

Use it

Look up 42291-232 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42291-232 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42291-232. 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.