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