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INON
INON - 49873-045-01 - (aluminum hydroxide, magnesium carbonate, sodium bicarbonate)
Drug Information of INON
| Product NDC: | 49873-045 |
| Proprietary Name: | INON |
| Non Proprietary Name: | aluminum hydroxide, magnesium carbonate, sodium bicarbonate |
| Active Ingredient(s): | 400; 400; 700 mg/1.92g; mg/1.92g; mg/1.92g & nbsp; aluminum hydroxide, magnesium carbonate, sodium bicarbonate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GRANULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of INON
| Product NDC: | 49873-045 |
| Labeler Name: | Sato Pharmaceutical Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19890531 |
Package Information of INON
| Package NDC: | 49873-045-01 |
| Package Description: | 12 PACKET in 1 CARTON (49873-045-01) > 1.92 g in 1 PACKET |
NDC Information of INON
| NDC Code | 49873-045-01 |
| Proprietary Name | INON |
| Package Description | 12 PACKET in 1 CARTON (49873-045-01) > 1.92 g in 1 PACKET |
| Product NDC | 49873-045 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | aluminum hydroxide, magnesium carbonate, sodium bicarbonate |
| Dosage Form Name | GRANULE |
| Route Name | ORAL |
| Start Marketing Date | 19890531 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Sato Pharmaceutical Co., Ltd. |
| Substance Name | ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE; SODIUM BICARBONATE |
| Strength Number | 400; 400; 700 |
| Strength Unit | mg/1.92g; mg/1.92g; mg/1.92g |
| Pharmaceutical Classes |
