Nitrofurantoin
NDC 16571-888, Nitrofurantoin, suspension, from Rising Pharma Holdings, Inc..
- Product NDC
- 16571-888
- Status
- Listed
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- SUSPENSION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA009175
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/16571-888 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- NITROFURANTOIN50 mg/5mL
Pharmacologic classes
Nitrofuran Antibacterial [EPC]; Nitrofurans [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 16571-888-06 | 16571088806 | 1 BOTTLE in 1 CARTON (16571-888-06) / 60 mL in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/89095f4d-e142-465e-b378-da24f6eeaf2b
Use it
Look up 16571-888 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/16571-888 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 16571-888. 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.