NDC 0186-1990
Pulmicort Respules 1 mg per 2 mL suspension
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
- Jan 11, 2013 · Class III · AstraZeneca LP
Does Not Meet Monograph: Budesonide may be slightly above or below the specification range.
Lots: Lot/Exp date: AH0054 Exp 5/14; AK0125 Exp 7/14 - Jan 11, 2013 · Class III · AstraZeneca LP
Does Not Meet Monograph: Budesonide may be slightly above or below the specification range.
Lots: Lot/Exp Date: YP0035 11/13; YP0140 12/13; YP0136 12/13; AB0077 2/14; AH0133 5/14
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: every company that makes it
- Form
- suspension, respiratory (inhalation)
- Strength
- 1 mg per 2 mL
- Approval
- NDA NDA020929
- On the market since
- Sep 17, 2007
- Package NDCs
0186-1990-04- Official label
- DailyMed (National Library of Medicine), updated Oct 11, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?