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Feverall Infants

NDC 51672-2114, Acetaminophen, suppository, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-2114
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
SUPPOSITORY
Route
RECTAL
Product type
HUMAN OTC DRUG
Marketing category
NDA
Application
NDA018337
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-2114 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACETAMINOPHEN80 mg/1
Package NDCNDC-11Package
51672-2114-2516722114026 BLISTER PACK in 1 CARTON (51672-2114-2) / 1 SUPPOSITORY in 1 BLISTER PACK (51672-2114-0)
51672-2114-45167221140450 BLISTER PACK in 1 CARTON (51672-2114-4) / 1 SUPPOSITORY in 1 BLISTER PACK (51672-2114-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 51672211402

    GET /v1/drugs/nadac/51672211402

Use it

Look up 51672-2114 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-2114 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-2114. 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.