NDC 63868-711 Ranitidine
NDC Product Code 63868-711
Proprietary Name: Ranitidine 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.
Drug Use Information
Drug Use InformationThe drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
- This product is used as acid reducer
Product Characteristics
Color(s):
PINK (C48328)
Shape: ROUND (C48348)
Size(s):
8 MM
Imprint(s):
OR;606
Score: 1
NDC Code Structure
- 63868 - Chain Drug Marketing Association Inc.
- 63868-711 - Ranitidine
NDC 63868-711-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
NDC 63868-711-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE
NDC Product Information
Ranitidine with NDC 63868-711 is product labeled by Chain Drug Marketing Association Inc.. The product's dosage form is and is administered via form.
RxNorm Crosswalk
What is RxNorm?RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.
The RxNorm Crosswalk for this NDC code indicates a single concept unique identifier (RXCUI) is associated with this product:
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.
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: Chain Drug Marketing Association Inc.
Labeler Code: 63868
Start Marketing Date: 07-10-2012 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: 12-31-2019 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...
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Ranitidine Product Label Images
Ranitidine 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
- Active Ingredient (In Each Tablet)
- Purpose
- Uses
- Warnings
- Do Not Use
- Ask A Doctor Before Use If You Have
- Stop Use And Ask A Doctor If
- If Pregnant Or Breast-Feeding
- Keep Out Of Reach Of Children.
- Directions
- Other Information
- Inactive Ingredients
- Questions?
Active Ingredient (In Each Tablet)
Ranitidine 75 mg (as ranitidine hydrochloride USP, 84 mg)
Purpose
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
- Frequent chest painfrequent wheezing, particularly with heartburnunexplained weight lossnausea or vomitingstomach painhad 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 lightheadedness
Stop Use And Ask A Doctor If
- Your heartburn continues or worsensyou need to take this product for more than 14 days
If Pregnant Or Breast-Feeding
Ask a health professional before use.
Keep Out Of Reach Of Children.
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
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)children under 12 years: ask a doctor
Other Information
- TAMPER EVIDENT: DO NOT USE IF THE CARTON OR PRINTED FOIL UNDER CAP IS OPEN OR TORN.store at 20° - 25° C (68° - 77° F)avoid excessive heat or humiditythis product is sodium and sugar free
Inactive Ingredients
Colloidal silicon dioxide, croscarmellose sodium, hypromellose, iron oxide red, magnesium stearate, microcrystalline cellulose, polyethylene glycol 400, talc, titanium dioxide
Questions?
Call 1-800-406-7984
* Please review the disclaimer below.