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NDC 51655-0697-51 Cimetidine 400 mg/1 Details

Cimetidine 400 mg/1

Cimetidine is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals. 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: 51655-0697-51
Last Updated: 04/21/2024
MedLinePlus Full Drug Details: Cimetidine

Product Information

NDC	51655-0697
Product ID	51655-697_db481bcd-d1c8-a7b2-e053-2995a90a2f2c
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	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	400
Active Ingredient Units	mg/1
Substance Name	CIMETIDINE
Labeler Name	Northwind Pharmaceuticals
Pharmaceutical Class	Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA074246
Listing Certified Through	2024-12-31

Package

NDC 51655-0697-51 (51655069751)

Pricing Information	N/A
NDC Package Code	51655-697-51
Billing NDC	51655069751
Package	40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-697-51)
Marketing Start Date	2021-04-01
NDC Exclude Flag	N