Phenazopyridine Hydrochloride
NDC 68788-7981, Phenazopyridine, tablet, from Preferred Pharmaceuticals Inc..
- Product NDC
- 68788-7981
- Status
- Listed
- Labeler
- Preferred Pharmaceuticals 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/68788-7981 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PHENAZOPYRIDINE HYDROCHLORIDE100 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68788-7981-1 | 68788798101 | 15 TABLET in 1 BOTTLE (68788-7981-1) |
| 68788-7981-2 | 68788798102 | 20 TABLET in 1 BOTTLE (68788-7981-2) |
| 68788-7981-6 | 68788798106 | 6 TABLET in 1 BOTTLE (68788-7981-6) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/132cc592-6b03-4b75-bf39-df476fb9dc81
Use it
Look up 68788-7981 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68788-7981 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68788-7981. 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.