NDC 54868-5974
Ipratropium Bromide and Albuterol Sulfate 3 mg / 0.5 mg solution
On the label: Physicians Total Care, Inc.. It's repackaged from NDC 0185-7322, made by Eon Labs, Inc. (Ipratropium Bromide and 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. 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 Physicians Total Care, Inc. names for other drugs.
Product details
- Generic drug
- Albuterol and Ipratropium: every company that makes it
- Form
- solution
- Strength
- 3 mg / 0.5 mg
- Approval
- NDA NDA020950
- On the market since
- Dec 18, 2008
- Package NDCs
54868-5974-0- Official label
- DailyMed (National Library of Medicine), updated Nov 5, 2010
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?