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NDC 69618-0054-42 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 RELIABLE 1 LABORATORIES LLC. The primary component is OMEPRAZOLE MAGNESIUM.

MedlinePlus Drug Summary

Prescription omeprazole is used alone or with other medications 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 omeprazole is used to treat damage from GERD in adults and children 1 month of age and older. Prescription omeprazole is used to allow the esophagus to heal and prevent further damage to the esophagus in adults and children 1 year of age and older with GERD. Prescription omeprazole is also used to treat conditions in which the stomach produces too much acid such as Zollinger-Ellison syndrome in adults. Prescription omeprazole is also used to treat ulcers (sores in the lining of the stomach or intestine) and it is also used with other medications to treat and prevent the return of ulcers caused by a certain type of bacteria (H. pylori) in adults. Nonprescription (over-the-counter) omeprazole is used to treat frequent heartburn (heartburn that occurs at least 2 or more days a week) in adults. Omeprazole is in a class of medications called proton-pump inhibitors. It works by decreasing the amount of acid made in the stomach.

Related Packages: 69618-0054-42
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Omeprazole

Product Information

NDC	69618-0054
Product ID	69618-054_ba632dd1-c85a-49c0-88a6-6d10ddbff1af
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	Omeprazole
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, DELAYED RELEASE
Route	ORAL
Active Ingredient Strength	20
Active Ingredient Units	mg/1
Substance Name	OMEPRAZOLE MAGNESIUM
Labeler Name	RELIABLE 1 LABORATORIES 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	ANDA206877
Listing Certified Through	2024-12-31

Package

NDC 69618-0054-42 (69618005442)

Pricing Information	N/A
NDC Package Code	69618-054-42
Billing NDC	69618005442
Package	3 BOTTLE in 1 CARTON (69618-054-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
Marketing Start Date	2021-03-11
NDC Exclude Flag	N