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Butalbital and Acetaminophen

NDC 68682-306, Butalbital and Acetaminophen tablets, tablet, from Oceanside Pharmaceuticals.

Product NDC
68682-306
Status
Listed
Labeler
Oceanside Pharmaceuticals
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090956
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68682-306 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUTALBITAL50 mg/1
  • ACETAMINOPHEN300 mg/1

Pharmacologic classes

Barbiturate [EPC]; Barbiturates [CS]

Package NDCNDC-11Package
68682-306-0168682030601100 TABLET in 1 BOTTLE, PLASTIC (68682-306-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d2213ffd-18f6-45f5-9af7-690a977562c4

Use it

Look up 68682-306 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68682-306 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68682-306. 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.