Dehydrated Alcohol
NDC 51991-999, Alcohol, injection, solution, from Breckenridge Pharmaceutical Inc.
- Product NDC
- 51991-999
- Status
- Listed
- Labeler
- Breckenridge Pharmaceutical Inc
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRA-ARTERIAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA219444
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51991-999 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ALCOHOL1 mL/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 51991-999-17 | 51991099917 | 10 VIAL, GLASS in 1 CARTON (51991-999-17) / 5 mL in 1 VIAL, GLASS (51991-999-75) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/be10b253-d72a-4f57-aa27-94c70ae8aed3
Use it
Look up 51991-999 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51991-999 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51991-999. 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.