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Phenobarbital

NDC 51672-5334, Phenobarbital, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-5334
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-5334 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PHENOBARBITAL100 mg/1
Package NDCNDC-11Package
51672-5334-151672533401100 TABLET in 1 BOTTLE, PLASTIC (51672-5334-1)
51672-5334-3516725334031000 TABLET in 1 BOTTLE, PLASTIC (51672-5334-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fa09b4f2-edb0-4594-a2d2-b16f7b9686b4

Use it

Look up 51672-5334 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-5334 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-5334. 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.