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Acetaminophen and Codeine

NDC 76420-103, Acetaminophen and Codeine, tablet, from Asclemed USA, Inc..

Product NDC
76420-103
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040779
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-103 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACETAMINOPHEN300 mg/1
  • CODEINE PHOSPHATE30 mg/1

Pharmacologic classes

Full Opioid Agonists [MoA]; Opioid Agonist [EPC]

Package NDCNDC-11Package
76420-103-03764200103033 TABLET in 1 BOTTLE (76420-103-03)
76420-103-107642001031010 TABLET in 1 BOTTLE (76420-103-10)
76420-103-207642001032020 TABLET in 1 BOTTLE (76420-103-20)
76420-103-307642001033030 TABLET in 1 BOTTLE (76420-103-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3f83ba75-9415-4ace-9416-04d666c005a2

Use it

Look up 76420-103 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-103 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-103. 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.