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PEPCID AC
PEPCID AC - 16837-855-49 - (Famotidine)
Drug Information of PEPCID AC
| Product NDC: | 16837-855 |
| Proprietary Name: | PEPCID AC |
| Non Proprietary Name: | Famotidine |
| Active Ingredient(s): | 20 mg/1 & nbsp; Famotidine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PEPCID AC
| Product NDC: | 16837-855 |
| Labeler Name: | McNeil Consumer Pharmaceuticals Co. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA020325 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030901 |
Package Information of PEPCID AC
| Package NDC: | 16837-855-49 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (16837-855-49) > 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
NDC Information of PEPCID AC
| NDC Code | 16837-855-49 |
| Proprietary Name | PEPCID AC |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (16837-855-49) > 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| Product NDC | 16837-855 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Famotidine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20030901 |
| Marketing Category Name | NDA |
| Labeler Name | McNeil Consumer Pharmaceuticals Co. |
| Substance Name | FAMOTIDINE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
