Skip to Content

APTIDINE 75

Dosage form: tablet
Ingredients: RANITIDINE HYDROCHLORIDE 75mg
Labeler: A P J Laboratories Limited
NDC Code: 46084-031

RANITIDINE HYDROCHLORIDE

Acid reducer

In case of overdose, get medical help or contact a Poison Control Center right away.

relieves heartburn associated with acid indigestion and sour stomach
prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain foods and beverages

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

adults and children 12 years and over:

to relieve symptoms, swallow 1 tablet with a glass of water
to prevent symptoms, swallow 1 tablet with a glass of water 30 to 60 minutes before eating food or drinking beverages that cause heartburn
can be used up to twice daily (do not take more than 2 tablets in 24 hours)

children under 12 years: ask a doctor







CELLULOSE, MICROCRYSTALLINE

STARCH, CORN


POVIDONE K30


METHYLPARABEN


MAGNESIUM STEARATE

TALC


SODIUM STARCH GLYCOLATE TYPE A POTATO


SILICON DIOXIDE

APTIDINE  75
ranitidine hydrochloride tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46084-031
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RANITIDINE HYDROCHLORIDE (RANITIDINE) RANITIDINE75 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE80 mg
STARCH, CORN30 mg
POVIDONE K3010 mg
METHYLPARABEN3 mg
MAGNESIUM STEARATE20 mg
TALC30 mg
SODIUM STARCH GLYCOLATE TYPE A POTATO40 mg
SILICON DIOXIDE1 mg
Product Characteristics
ColorpinkScoreno score
ShapeROUNDSize10mm
FlavorImprint Code75MG
Contains    
Packaging
#Item CodePackage Description
1NDC:46084-031-15120 TABLET (TABLET) in 1 BLISTER PACK
2NDC:46084-031-1460 TABLET (TABLET) in 1 BLISTER PACK
3NDC:46084-031-1336 TABLET (TABLET) in 1 BLISTER PACK
4NDC:46084-031-1212 TABLET (TABLET) in 1 BLISTER PACK
5NDC:46084-031-115 TABLET (TABLET) in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07513203/01/2013
Labeler - A P J Laboratories Limited (677378339)
Registrant - A P J Laboratories Limited (677378339)
Establishment
NameAddressID/FEIOperations
A P J Laboratories Limited677378339manufacture(46084-031)

Revised: 02/2013
 
A P J Laboratories Limited

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

Hide