NDC 0487-0301
Albuterol Sulfate 0.63 mg per 3 mL solution
On the label: Nephron Pharmaceuticals Corporation.
Where it's 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 |
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
- Albuterol: every company that makes it
- Form
- solution, respiratory (inhalation)
- Strength
- 0.63 mg per 3 mL
- Approval
- ANDA ANDA076355
- On the market since
- Mar 31, 2010
- Package NDCs
0487-0301-010487-0301-02- Official label
- DailyMed (National Library of Medicine), updated Apr 6, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?