Product NDC: | 16837-298 |
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) |
Product NDC: | 16837-298 |
Labeler Name: | McNeil Consumer Pharmaceuticals Co. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA020958 |
Marketing Category: | NDA |
Start Marketing Date: | 20090301 |
Package NDC: | 16837-298-36 |
Package Description: | 35 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (16837-298-36) |
NDC Code | 16837-298-36 |
Proprietary Name | Pepcid Complete |
Package Description | 35 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (16837-298-36) |
Product NDC | 16837-298 |
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 |