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NDC 62135-0631-90 CIMETIDINE 300 mg/1 Details

CIMETIDINE 300 mg/1

CIMETIDINE is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Chartwell RX, LLC. The primary component is CIMETIDINE.

MedlinePlus Drug Summary

Cimetidine is used to treat ulcers; gastroesophageal reflux disease (GERD), a condition in which backward flow of acid from the stomach causes heartburn and injury of the food pipe (esophagus); and conditions where the stomach produces too much acid, such as Zollinger-Ellison syndrome. Over-the-counter cimetidine is used to prevent and treat symptoms of heartburn associated with acid indigestion and sour stomach. Cimetidine is in a class of medications called H2 blockers. It decreases the amount of acid made in the stomach.

Related Packages: 62135-0631-90
Last Updated: 04/28/2024
MedLinePlus Full Drug Details: Cimetidine

Product Information

NDC	62135-0631
Product ID	62135-631_0337689b-c5d5-d881-e063-6394a90aaec9
Associated GPIs
GCN Sequence Number	011666
GCN Sequence Number Description	cimetidine TABLET 300 MG ORAL
HIC3	Z2D
HIC3 Description	HISTAMINE H2-RECEPTOR INHIBITORS
GCN	46751
HICL Sequence Number	004518
HICL Sequence Number Description	CIMETIDINE
Brand/Generic	Generic
Proprietary Name	CIMETIDINE
Proprietary Name Suffix	n/a
Non-Proprietary Name	CIMETIDINE
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	300
Active Ingredient Units	mg/1
Substance Name	CIMETIDINE
Labeler Name	Chartwell RX, LLC
Pharmaceutical Class	Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA074329
Listing Certified Through	2024-12-31

Package

NDC 62135-0631-90 (62135063190)

Pricing Information	N/A
NDC Package Code	62135-631-90
Billing NDC	62135063190
Package	90 TABLET, FILM COATED in 1 BOTTLE (62135-631-90)
Marketing Start Date	2023-08-15
NDC Exclude Flag	N