NDC 61919-509
Nexium 40 mg capsule, delayed release
On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from AstraZeneca Pharmaceuticals LP's NDC 0186-5040.
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 AstraZeneca Pharmaceuticals LP names for other drugs.
Repackaging site
- Direct Rx, Dawsonville, GA, United States · repackages it and relabels it
Recalls
- Jul 2, 2012 · Class III · ASTRA ZENECA Lp
Adulterated Presence of Foreign Tablets/Capsules: Some bottles may contain a small number of Nexium 20 mg capsules intended for the Japanese market in addtion to Nexium 40 mg capsules.
Lots: Lot #: H008328, Exp 11/14
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Esomeprazole: every company that makes it
- Form
- capsule, delayed release
- Strength
- 40 mg
- Approval
- NDA NDA021153
- On the market since
- Jan 1, 2014
- Package NDCs
61919-509-3061919-509-60- Official label
- DailyMed (National Library of Medicine), updated Mar 28, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?