NDC 42023-146
Dexmedetomidine Hydrochloride 100 ug per 1 mL injection, solution, concentrate
On the label: ENDO USA, Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants ENDO USA, Inc. names for other drugs.
Product details
- Generic drug
- Dexmedetomidine: every company that makes it
- Form
- injection, solution, concentrate, intravenous
- Strength
- 100 ug per 1 mL
- Approval
- ANDA ANDA203972
- On the market since
- Aug 19, 2014
- Package NDCs
42023-146-25- Official label
- DailyMed (National Library of Medicine), updated Feb 1, 2024
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