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GERI-LANTA MAXIMUM STRENGTH
GERI-LANTA MAXIMUM STRENGTH - 57896-619-12 - (aluminum hydroxide, magnesium hydroxide, dimethicone)
Drug Information of GERI-LANTA MAXIMUM STRENGTH
| Product NDC: | 57896-619 |
| Proprietary Name: | GERI-LANTA MAXIMUM STRENGTH |
| Non Proprietary Name: | aluminum hydroxide, magnesium hydroxide, dimethicone |
| Active Ingredient(s): | 400; 40; 400 mg/5mL; mg/5mL; mg/5mL & nbsp; aluminum hydroxide, magnesium hydroxide, dimethicone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GERI-LANTA MAXIMUM STRENGTH
| Product NDC: | 57896-619 |
| Labeler Name: | Geri-Care Pharmaceuticals, Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20000101 |
Package Information of GERI-LANTA MAXIMUM STRENGTH
| Package NDC: | 57896-619-12 |
| Package Description: | 355 mL in 1 BOTTLE (57896-619-12) |
NDC Information of GERI-LANTA MAXIMUM STRENGTH
| NDC Code | 57896-619-12 |
| Proprietary Name | GERI-LANTA MAXIMUM STRENGTH |
| Package Description | 355 mL in 1 BOTTLE (57896-619-12) |
| Product NDC | 57896-619 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | aluminum hydroxide, magnesium hydroxide, dimethicone |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20000101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Geri-Care Pharmaceuticals, Corp |
| Substance Name | ALUMINUM HYDROXIDE; DIMETHICONE; MAGNESIUM HYDROXIDE |
| Strength Number | 400; 40; 400 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
