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Butalbital, Acetaminophen and Caffeine

NDC 51672-4222, butalbital, acetaminophen, and caffeine, capsule, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4222
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213046
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4222 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUTALBITAL50 mg/1
  • ACETAMINOPHEN300 mg/1
  • CAFFEINE40 mg/1

Pharmacologic classes

Barbiturate [EPC]; Barbiturates [CS]; Central Nervous System Stimulant [EPC]; Central Nervous System Stimulation [PE]; Methylxanthine [EPC]; Xanthines [CS]

Package NDCNDC-11Package
51672-4222-151672422201100 CAPSULE in 1 BOTTLE (51672-4222-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a68de112-f5af-49ba-a8a8-3adbaa7df36e

  • NADAC price for package 51672422201

    GET /v1/drugs/nadac/51672422201

Use it

Look up 51672-4222 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4222 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4222. 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.