NDC 0186-5020 – Nexium

Esomeprazole Magnesium Trihydrate 20 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug 1 recall

Product NDC0186-5020

Product details

Brand name
Nexium
Generic name
Esomeprazole magnesium
Labeler
AstraZeneca Pharmaceuticals LP
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
NDA · NDA021153
Marketed since
March 19, 2001
Listing expires
December 31, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Nexium →

Package NDC codes (2)

Package NDCDescriptionSince
0186-5020-3130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0186-5020-31)Mar 19, 2001
0186-5020-5490 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0186-5020-54)Mar 19, 2001

Recalls mentioning this NDC

Other Nexium products