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
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 NDC | NDC-11 | Package |
|---|---|---|
| 63304-506-01 | 63304050601 | 100 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 https://api.healthcare.dev/v1/drugs/ndc/63304-506 \ -H "Authorization: Bearer $HDEV_API_KEY"
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.