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NDC 59726-0056-42 Acid Reducer 20 mg/1 Details

Acid Reducer 20 mg/1

Acid Reducer is a ORAL TABLET, DELAYED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by P & L Development, LLC. The primary component is ESOMEPRAZOLE MAGNESIUM.

MedlinePlus Drug Summary

Prescription esomeprazole is used to treat the symptoms of gastroesophageal reflux disease (GERD), a condition in which backward flow of acid from the stomach causes heartburn and possible injury of the esophagus (the tube between the throat and stomach) in adults and children 1 year of age and older. Prescription esomeprazole is used to treat damage from GERD in adults and children 1 month of age and older. Prescription esomeprazole is used to allow the esophagus to heal and prevent further damage to the esophagus in adults with GERD. Prescription esomeprazole is also used to decrease the chance that people who are taking nonsteroidal anti-inflammatory drugs (NSAIDs) will develop ulcers (sores in the lining of the stomach or intestine) in adults. It is also used with other medications to treat and prevent the return of stomach ulcers caused by a certain type of bacteria (H. pylori) in adults. Prescription esomeprazole is also used to treat conditions in which the stomach produces too much acid such as Zollinger-Ellison syndrome in adults. Nonprescription (over-the-counter) esomeprazole is used to treat frequent heartburn (heartburn that occurs at least 2 or more days a week) in adults. Esomeprazole is in a class of medications called proton pump inhibitors. It works by decreasing the amount of acid made in the stomach.

Related Packages: 59726-0056-42
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Esomeprazole

Product Information

NDC	59726-0056
Product ID	59726-056_6e82983e-c3bf-42e2-a9b0-eb9cb86cb935
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Acid Reducer
Proprietary Name Suffix	n/a
Non-Proprietary Name	Esomeprazole magnesium
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, DELAYED RELEASE
Route	ORAL
Active Ingredient Strength	20
Active Ingredient Units	mg/1
Substance Name	ESOMEPRAZOLE MAGNESIUM
Labeler Name	P & L Development, LLC
Pharmaceutical Class	Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA212088
Listing Certified Through	2024-12-31

Package

NDC 59726-0056-42 (59726005642)

Pricing Information	N/A
NDC Package Code	59726-056-42
Billing NDC	59726005642
Package	3 BOTTLE, PLASTIC in 1 CARTON (59726-056-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
Marketing Start Date	2020-12-31
NDC Exclude Flag	N