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NDC 57841-1301, naloxegol oxalate, tablet, film coated, from RedHill Biopharma Ltd.

Product NDC
57841-1301
Status
Listed
Labeler
RedHill Biopharma Ltd
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA204760
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57841-1301 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NALOXEGOL OXALATE25 mg/1

Pharmacologic classes

Opioid Antagonist [EPC]; Opioid Antagonists [MoA]

Package NDCNDC-11Package
57841-1301-15784113010130 TABLET, FILM COATED in 1 BOTTLE (57841-1301-1)
57841-1301-25784113010290 TABLET, FILM COATED in 1 BOTTLE (57841-1301-2)
57841-1301-35784113010310 BLISTER PACK in 1 CARTON (57841-1301-3) / 10 TABLET, FILM COATED in 1 BLISTER PACK
57841-1301-4578411301041 BLISTER PACK in 1 CARTON (57841-1301-4) / 3 TABLET, FILM COATED in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/300a6474-ebcd-4404-8040-48fdcfcc1635

Use it

Look up 57841-1301 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57841-1301 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57841-1301. 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.