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Butalbital And Acetaminophen

NDC 68047-721, butalbital and acetaminophen, tablet, from Larken Laboratories, Inc..

Product NDC
68047-721
Status
Listed
Labeler
Larken Laboratories, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203484
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68047-721 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUTALBITAL50 mg/1
  • ACETAMINOPHEN325 mg/1

Pharmacologic classes

Barbiturate [EPC]; Barbiturates [CS]

Package NDCNDC-11Package
68047-721-0168047072101100 TABLET in 1 BOTTLE (68047-721-01)
68047-721-306804707213030 TABLET in 1 BOTTLE (68047-721-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/326c83fc-afed-45ad-9c87-f47968fa1d2a

  • NADAC price for package 68047072101

    GET /v1/drugs/nadac/68047072101

Use it

Look up 68047-721 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68047-721 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68047-721. 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.