NDC 50090-4185
Ipratropium Bromide 0.5 mg per 2.5 mL solution
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Nephron Pharmaceuticals Corporation's NDC 0487-9801.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Nephron SC, LLC | West Columbia, SC, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyAug 22, 2025 · 26 inspections, 10 with FDA action |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · relabels it
Recalls
- Apr 13, 2022 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
cGMP deviations: Temperature abuse
Lots: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ipratropium: every company that makes it
- Form
- solution
- Strength
- 0.5 mg per 2.5 mL
- Approval
- ANDA ANDA075562
- On the market since
- Sep 27, 2001
- Package NDCs
50090-4185-0- Official label
- DailyMed (National Library of Medicine), updated Oct 28, 2026
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