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Pepcid Complete
Pepcid Complete - 16837-891-50 - (famotidine, calcium carbonate, and magnesium hydroxide)
Drug Information of Pepcid Complete
| Product NDC: | 16837-891 |
| Proprietary Name: | Pepcid Complete |
| Non Proprietary Name: | famotidine, calcium carbonate, and magnesium hydroxide |
| Active Ingredient(s): | 800; 10; 165 mg/1; mg/1; mg/1 & nbsp; famotidine, calcium carbonate, and magnesium hydroxide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pepcid Complete
| Product NDC: | 16837-891 |
| Labeler Name: | McNeil Consumer Pharmaceuticals Co. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA020958 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090301 |
Package Information of Pepcid Complete
| Package NDC: | 16837-891-50 |
| Package Description: | 50 TABLET, CHEWABLE in 1 BOTTLE (16837-891-50) |
NDC Information of Pepcid Complete
| NDC Code | 16837-891-50 |
| Proprietary Name | Pepcid Complete |
| Package Description | 50 TABLET, CHEWABLE in 1 BOTTLE (16837-891-50) |
| Product NDC | 16837-891 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | famotidine, calcium carbonate, and magnesium hydroxide |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20090301 |
| Marketing Category Name | NDA |
| Labeler Name | McNeil Consumer Pharmaceuticals Co. |
| Substance Name | CALCIUM CARBONATE; FAMOTIDINE; MAGNESIUM HYDROXIDE |
| Strength Number | 800; 10; 165 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
