Phenazopyridine Hydrochloride
NDC 70518-3443, Phenazopyridine, tablet, from REMEDYREPACK INC..
- Product NDC
- 70518-3443
- Status
- Listed
- Labeler
- REMEDYREPACK 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/70518-3443 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PHENAZOPYRIDINE HYDROCHLORIDE100 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70518-3443-1 | 70518344301 | 12 TABLET in 1 BOTTLE, PLASTIC (70518-3443-1) |
| 70518-3443-3 | 70518344303 | 6 TABLET in 1 BOTTLE, PLASTIC (70518-3443-3) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/f6829698-b12e-484d-a322-d2f68586e637
Use it
Look up 70518-3443 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3443 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-3443. 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.