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Gelusil
Gelusil - 65197-300-20 - (aluminum hydroxide dried gel and magnesium hydroxide and simethicone)
Drug Information of Gelusil
| Product NDC: | 65197-300 |
| Proprietary Name: | Gelusil |
| Non Proprietary Name: | aluminum hydroxide dried gel and magnesium hydroxide and simethicone |
| Active Ingredient(s): | 200; 24; 200; 1 mg/1; mg/1; mg/1; mg/1 & nbsp; aluminum hydroxide dried gel and magnesium hydroxide and simethicone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Gelusil
| Product NDC: | 65197-300 |
| Labeler Name: | WellSpring Pharmaceutical Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080924 |
Package Information of Gelusil
| Package NDC: | 65197-300-20 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (65197-300-20) > 10 TABLET, CHEWABLE in 1 BLISTER PACK |
NDC Information of Gelusil
| NDC Code | 65197-300-20 |
| Proprietary Name | Gelusil |
| Package Description | 2 BLISTER PACK in 1 CARTON (65197-300-20) > 10 TABLET, CHEWABLE in 1 BLISTER PACK |
| Product NDC | 65197-300 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | aluminum hydroxide dried gel and magnesium hydroxide and simethicone |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20080924 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | WellSpring Pharmaceutical Corporation |
| Substance Name | ALUMINUM HYDROXIDE; DIMETHICONE 410; MAGNESIUM HYDROXIDE; SILICON DIOXIDE |
| Strength Number | 200; 24; 200; 1 |
| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
