NDC 0310-7370
Budesonide and Formoterol Fumarate Dihydrate 160 ug / 4.5 ug aerosol
On the label: AstraZeneca Pharmaceuticals LP.
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 AstraZeneca Pharmaceuticals LP names for other drugs.
Recalls
- Mar 15, 2021 · Class II · Cardinal Health Inc.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots: 2000655C00
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Budesonide and Formoterol: every company that makes it
- Form
- aerosol, respiratory (inhalation)
- Strength
- 160 ug / 4.5 ug
- Approval
- NDA authorized generic NDA021929
- On the market since
- Jan 3, 2020
- Package NDCs
0310-7370-20- Official label
- DailyMed (National Library of Medicine), updated Jul 24, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?