| Product NDC: | 59779-546 | 
| Proprietary Name: | complete | 
| Non Proprietary Name: | Famotidine, Calcium Carbonate, Magnesium Hydroxide | 
| Active Ingredient(s): | 800; 10; 165 mg/1; mg/1; mg/1 & nbsp; Famotidine, Calcium Carbonate, Magnesium Hydroxide | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET, CHEWABLE | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 59779-546 | 
| Labeler Name: | CVS Pharmacy | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | ANDA077355 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20080826 | 
| Package NDC: | 59779-546-65 | 
| Package Description: | 30 TABLET, CHEWABLE in 1 BOTTLE (59779-546-65) | 
| NDC Code | 59779-546-65 | 
| Proprietary Name | complete | 
| Package Description | 30 TABLET, CHEWABLE in 1 BOTTLE (59779-546-65) | 
| Product NDC | 59779-546 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Famotidine, Calcium Carbonate, Magnesium Hydroxide | 
| Dosage Form Name | TABLET, CHEWABLE | 
| Route Name | ORAL | 
| Start Marketing Date | 20080826 | 
| Marketing Category Name | ANDA | 
| Labeler Name | CVS Pharmacy | 
| Substance Name | CALCIUM CARBONATE; FAMOTIDINE; MAGNESIUM HYDROXIDE | 
| Strength Number | 800; 10; 165 | 
| Strength Unit | mg/1; mg/1; mg/1 | 
| Pharmaceutical Classes |