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Codeine Sulfate

NDC 0527-1727, Codeine Sulfate, tablet, from Lannett Company, Inc..

Product NDC
0527-1727
Status
Listed
Labeler
Lannett Company, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203046
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0527-1727 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CODEINE SULFATE15 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
0527-1727-91005271727914 BLISTER PACK in 1 CARTON (0527-1727-91) / 25 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5819bdf7-300e-45b8-8f3a-447b53656293

Use it

Look up 0527-1727 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0527-1727 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0527-1727. 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.