Zantac 150

Active Ingredient(s): Ranitidine Hydrochloride
FDA Approved: * June 9, 1983
Pharm Company: * GLAXOSMITHKLINE
Category: Ulcer

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".



Zantac 150 Overview

Ranitidine, sold under the trade name Zantac among others, is a medication which decreases stomach acid production.[1] It is commonly used in treatment of peptic ulcer disease, gastroesophageal reflux disease, and Zollinger–Ellison syndrome.[1] There is also tentative evidence of benefit for hives.[3] It can be taken by mouth, by injection into a muscle, or into a vein.[1] Common side effects include headaches and pain or ...

Read more Zantac 150 Details
Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Ranitidine

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Possible Dosages for this and Related Drugs:

Ranitidine Hydrochloride
  • Capsule: 150mg, 300mg
  • Granule, Effervescent: 150mg, 150mg/packet
  • Injection: 1mg/ml, 25mg/ml
  • N/a: na
  • Solution: 15mg/ml
  • Syrup: 150mg/10ml, 15mg, 15mg/ml
  • Tablet: 150mg, 300mg, 75mg
  • Tablet, Effervescent: 150mg, 25mg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Zantac 150: (3 results)

Sorted by National Drug Code
  • 0597-0220 Zantac 150 150 mg Oral Tablet by Boehringer Ingelheim Promeco S.a. De C.v.
  • 50269-220 Zantac 150 150 mg Oral Tablet by Jc World Bell Wholesale Co., Inc.
  • 67751-151 Zantac 150 150 mg Oral Tablet by Navajo Manufacturing Company Inc.

Other drugs which contain Ranitidine Hydrochloride or a similar ingredient: (3 results)

Related Zantac 150 Topics:

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