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Pepcid AC
Pepcid AC - 16837-867-35 - (famotidine)
Drug Information of Pepcid AC
| Product NDC: | 16837-867 |
| Proprietary Name: | Pepcid AC |
| Non Proprietary Name: | famotidine |
| Active Ingredient(s): | 20 mg/1 & nbsp; famotidine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pepcid AC
| Product NDC: | 16837-867 |
| Labeler Name: | McNeil Consumer Pharmaceuticals Co. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA020801 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080201 |
Package Information of Pepcid AC
| Package NDC: | 16837-867-35 |
| Package Description: | 1 BOTTLE in 1 CARTON (16837-867-35) > 35 TABLET, CHEWABLE in 1 BOTTLE |
NDC Information of Pepcid AC
| NDC Code | 16837-867-35 |
| Proprietary Name | Pepcid AC |
| Package Description | 1 BOTTLE in 1 CARTON (16837-867-35) > 35 TABLET, CHEWABLE in 1 BOTTLE |
| Product NDC | 16837-867 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | famotidine |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20080201 |
| Marketing Category Name | NDA |
| Labeler Name | McNeil Consumer Pharmaceuticals Co. |
| Substance Name | FAMOTIDINE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
