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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)

 
A P J Laboratories Limited

Medically reviewed on Feb 21, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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