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pentazocine and naloxone

NDC 63304-506, pentazocine and naloxone, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
63304-506
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075523
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63304-506 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PENTAZOCINE50 mg/1
  • NALOXONE HYDROCHLORIDE.5 mg/1

Pharmacologic classes

Competitive Opioid Antagonists [MoA]; Opioid Antagonist [EPC]; Opioid Antagonists [MoA]; Partial Opioid Agonist/Antagonist [EPC]; Partial Opioid Agonists [MoA]

Package NDCNDC-11Package
63304-506-0163304050601100 TABLET in 1 BOTTLE (63304-506-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/41ebdaaf-3bbc-419f-b996-0341efc14623

Use it

Look up 63304-506 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63304-506 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63304-506. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.