NDC 72189-022
Albuterol Sulfate 2.5 mg per 3 mL solution
On the label: Direct Rx. It's repackaged from NDC 0591-3797, made by Actavis Pharma, Inc. (Albuterol Sulfate). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that relabels it). 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 Direct Rx names for other drugs.
Product details
- Generic drug
- Albuterol: every company that makes it
- Form
- solution
- Strength
- 2.5 mg per 3 mL
- Approval
- ANDA ANDA077839
- On the market since
- Oct 29, 2019
- Package NDCs
72189-022-25- Official label
- DailyMed (National Library of Medicine), updated Oct 29, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?