NDC 75834-230
Remifentanil hydrochloride 1 mg injection, powder, lyophilized, for solution
On the label: Pharmaceutical Associates, 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 Pharmaceutical Associates, Inc. names for other drugs.
Product details
- Generic drug
- Remifentanil: every company that makes it
- Form
- injection, powder, lyophilized, for solution
- Strength
- 1 mg
- Approval
- ANDA ANDA215635
- On the market since
- Sep 4, 2024
- Package NDCs
75834-230-0175834-230-10- Official label
- DailyMed (National Library of Medicine), updated Oct 2, 2026
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