Inon Ace - 49873-402-01 - (magnesium aluminosilicates, magnesium hydroxide, simethicone)

Alphabetical Index


Drug Information of Inon Ace

Product NDC: 49873-402
Proprietary Name: Inon Ace
Non Proprietary Name: magnesium aluminosilicates, magnesium hydroxide, simethicone
Active Ingredient(s): 200; 20; 60    g/1; mg/1; mg/1 & nbsp;   magnesium aluminosilicates, magnesium hydroxide, simethicone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Inon Ace

Product NDC: 49873-402
Labeler Name: Sato Pharmaceutical Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part331
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19951101

Package Information of Inon Ace

Package NDC: 49873-402-01
Package Description: 1 BOTTLE in 1 CARTON (49873-402-01) > 75 TABLET in 1 BOTTLE

NDC Information of Inon Ace

NDC Code 49873-402-01
Proprietary Name Inon Ace
Package Description 1 BOTTLE in 1 CARTON (49873-402-01) > 75 TABLET in 1 BOTTLE
Product NDC 49873-402
Product Type Name HUMAN OTC DRUG
Non Proprietary Name magnesium aluminosilicates, magnesium hydroxide, simethicone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19951101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Sato Pharmaceutical Co., Ltd.
Substance Name ALMASILATE; DIMETHICONE; MAGNESIUM HYDROXIDE
Strength Number 200; 20; 60
Strength Unit g/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Inon Ace


General Information