NDC 80425-0111

Nexium

Esomeprazole Magnesium 20mg

Nexium is a Oral Capsule, Delayed Release in the Human Prescription Drug category. It is labeled and distributed by Advanced Rx Pharmacy Of Tennessee, Llc. The primary component is Esomeprazole Magnesium Dihydrate.

• Product ID: 80425-0111_b5a6e7de-fded-a3b6-e053-2a95a90a5aa2
• NDC: 80425-0111
• Product Type: Human Prescription Drug
• Proprietary Name: Nexium
• Generic Name: Esomeprazole Magnesium 20mg
• Dosage Form: Capsule, Delayed Release
• Route of Administration: ORAL
• Marketing Start Date: 2016-04-21
• Marketing Category: ANDA / ANDA
• Application Number: ANDA205606
• Labeler Name: Advanced Rx Pharmacy of Tennessee, LLC
• Substance Name: ESOMEPRAZOLE MAGNESIUM DIHYDRATE
• Active Ingredient Strength: 20 mg/1
• Pharm Classes: Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 80425-0111-1

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0111-1)

• Marketing Start Date: 2016-04-21
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Nexium" or generic name "Esomeprazole Magnesium 20mg"

NDC	Brand Name	Generic Name
0186-4010	NEXIUM	Esomeprazole magnesium
0186-4020	NEXIUM	Esomeprazole magnesium
0186-4025	NEXIUM	Esomeprazole magnesium
0186-4040	NEXIUM	Esomeprazole magnesium
0186-4050	NEXIUM	Esomeprazole magnesium
21695-092	NEXIUM	NEXIUM
21695-091	NEXIUM	NEXIUM
0186-5040	NEXIUM	NEXIUM
0186-5020	NEXIUM	NEXIUM
50090-0742	NEXIUM	NEXIUM
49999-307	NEXIUM	NEXIUM
50436-3121	NEXIUM	NEXIUM
55154-9616	NEXIUM	NEXIUM
55700-046	NEXIUM	NEXIUM
61919-509	NEXIUM	NEXIUM
63629-3311	NEXIUM	NEXIUM
70518-2038	NEXIUM	NEXIUM
80425-0111	Nexium	Nexium