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Inon Ace
Inon Ace - 49873-403-01 - (magnesium aluminosilicate, magnesium hydroxide)
Drug Information of Inon Ace
| Product NDC: | 49873-403 |
| Proprietary Name: | Inon Ace |
| Non Proprietary Name: | magnesium aluminosilicate, magnesium hydroxide |
| Active Ingredient(s): | 250; 900 mg/30mL; mg/30mL & nbsp; magnesium aluminosilicate, magnesium hydroxide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Inon Ace
| Product NDC: | 49873-403 |
| Labeler Name: | Sato Pharmaceutical Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20000520 |
Package Information of Inon Ace
| Package NDC: | 49873-403-01 |
| Package Description: | 2 BOTTLE in 1 CARTON (49873-403-01) > 30 mL in 1 BOTTLE |
NDC Information of Inon Ace
| NDC Code | 49873-403-01 |
| Proprietary Name | Inon Ace |
| Package Description | 2 BOTTLE in 1 CARTON (49873-403-01) > 30 mL in 1 BOTTLE |
| Product NDC | 49873-403 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | magnesium aluminosilicate, magnesium hydroxide |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20000520 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Sato Pharmaceutical Co., Ltd. |
| Substance Name | MAGNESIUM HYDROXIDE; SILODRATE |
| Strength Number | 250; 900 |
| Strength Unit | mg/30mL; mg/30mL |
| Pharmaceutical Classes |
