NDC 51991-999
Dehydrated Alcohol 1 mL per 1 mL injection, solution
On the label: Breckenridge Pharmaceutical, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Immacule Lifesciences Private Limited | Solan, India | Makes it, tests it, packages it and labels it | Serious problems, FDA actionSep 18, 2025 · 3 inspections, 1 with FDA action |
| Megsan Labs Private Limited | Hyderabad, India | Tests it | Serious problems, FDA actionAug 22, 2025 · 4 inspections, 2 with FDA action |
| Merck Kommanditgesellschaft auf Aktien | Darmstadt, Germany | Tests it | Problems found, fixed voluntarilyOct 6, 2023 · 4 inspections |
| Reading Scientific Services Ltd | Reading, United Kingdom | Tests it | Problems found, fixed voluntarilyDec 15, 2023 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Alcohol: every company that makes it
- Form
- injection, solution, intra-arterial
- Strength
- 1 mL per 1 mL
- Approval
- ANDA ANDA219444
- On the market since
- Sep 23, 2025
- Package NDCs
51991-999-1751991-999-75- Official label
- DailyMed (National Library of Medicine), updated Aug 27, 2026
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