Phenobarbital
NDC 16571-675, Phenobarbital, liquid, from Rising Pharma Holdings, Inc..
- Product NDC
- 16571-675
- Status
- Listed
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- LIQUID
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- CIV
curl https://api.healthcare.dev/v1/drugs/ndc/16571-675 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PHENOBARBITAL20 mg/5mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 16571-675-16 | 16571067516 | 473 mL in 1 BOTTLE (16571-675-16) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/fe874f8a-4b56-4d2b-abf5-8742e2633a3bNADAC price for package 16571067516
GET /v1/drugs/nadac/16571067516
Use it
Look up 16571-675 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/16571-675 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 16571-675. 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.