NDC 68151-2584 Zantac 75

NDC Product Code 68151-2584

NDC CODE: 68151-2584

Proprietary Name: Zantac 75 What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Product Characteristics

Color(s):
PINK (C48328)
Shape: PENTAGON (5 SIDED) (C48346)
Size(s):
3 MM
Imprint(s):
Z;75
Score: 1

NDC Code Structure

  • 68151 - Carilion Materials Management

NDC 68151-2584-0

Package Description: 1 TABLET, COATED in 1 PACKAGE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Zantac 75 with NDC 68151-2584 is a product labeled by Carilion Materials Management. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates multiple RxCUI concepts are associated to this product: 312773 and 827183.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)
  • MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • TRIACETIN (UNII: XHX3C3X673)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Carilion Materials Management
Labeler Code: 68151
Start Marketing Date: 12-21-2006 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2018 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Information for Patients

Ranitidine

Ranitidine is pronounced as (ra ni' ti deen)

Why is ranitidine medication prescribed?
Ranitidine 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...
[Read More]

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Zantac 75 Product Label Images

Zantac 75 Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Drug Facts

Active ingredient (in each tablet)PurposeRanitidine 75 mg (as ranitidine hydrochloride 84 mg) . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . Acid reducer

Uses

  • Relieves heartburn associated with acid indigestion and
  • Sour stomachprevents heartburn associated with acid indigestion and
  • Sour stomach brought on by eating or drinking certain foods and beverages

Warnings

Allergy
alert: Do not use if you are allergic to ranitidine or other
acid reducers

Do Not Use

  • If you have trouble or pain swallowing food, vomiting with
  • Blood, or bloody or black stools. These may be signs of a serious
  • Condition. See your doctor.with other acid reducers

Ask A Doctor Before Use If You Have

  • Had heartburn over 3 months. This may be a sign of a more
  • Serious condition.heartburn with lightheadedness, sweating or dizzinesschest pain or shoulder pain with shortness of breath; sweating;
  • Pain spreading to arms, neck or shoulders; or lightheadednessfrequent chest painfrequent wheezing, particularly with heartburnunexplained weight lossnausea or vomitingstomach pain

Stop Use And Ask A Doctor If

  • Your heartburn continues or worsensyou need to take this product for more than 14 daysIf pregnant or breast-feeding, ask a health professional before use.

Directions

  • Adults and children 12 years and over:to relieve symptoms, swallow 1 tablet with
  • A glass of waterto prevent symptoms, swallow 1 tablet with
  • A glass of water 30 to 60 minutes before eating food
  • Or drinking beverages that cause heartburncan be used up to twice daily (do not take more than 2 tablets
  • In 24 hours)do not chew tabletchildren under 12 years: ask a doctor

Other Information

  • Do not use if printed foil under bottle cap is open or torn
  • (bottles)do not use if individual blister unit is open or torn (blisters)do not use if individual foil packet is open or torn (pouch)store at 20-25ºC (68-77ºF)avoid excessive heat or humiditythis product is sodium and sugar free

Inactive Ingredients

Hypromellose, magnesium stearate, microcrystalline
cellulose, iron oxide, titanium dioxide, triacetin

Questions?

Call 1-888-285-9159 (English/Spanish) M
– F, 8:30 – 5 EST, or visit www.zantacotc.com

Other

Read the directions, consumer information
leaflet and warnings before use. Keep the carton. It contains important
information.Distributed by: Boehringer Ingelheim (BI) Consumer Health Care ProductsDivision of BI Pharmaceuticals, Inc., Ridgefield, CT 06877© 2016, BI Pharmaceuticals, Inc. All rights reserved.Product of Spain. Manufactured in Mexico.

How Supplied

Product: 68151-2584NDC: 68151-2584-0 1 TABLET, COATED in a PACKAGE

* Please review the disclaimer below.