PHENAZOPYRIDINE HYDROCHLORIDE
NDC 64950-550, PHENAZOPYRIDINE HYDROCHLORIDE, tablet, from Genus Lifesciences Inc..
- Product NDC
- 64950-550
- Status
- Listed
- Labeler
- Genus Lifesciences Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/64950-550 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PHENAZOPYRIDINE HYDROCHLORIDE100 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 64950-550-01 | 64950055001 | 100 TABLET in 1 BOTTLE (64950-550-01) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/991b3b97-9cea-4c48-90a4-ebff55417d98
Use it
Look up 64950-550 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/64950-550 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 64950-550. 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.