Product NDC: | 65649-211 |
Proprietary Name: | PEPCID |
Non Proprietary Name: | FAMOTIDINE |
Active Ingredient(s): | 40 mg/5mL & nbsp; FAMOTIDINE |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER, FOR SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65649-211 |
Labeler Name: | Salix Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019527 |
Marketing Category: | NDA |
Start Marketing Date: | 19870601 |
Package NDC: | 65649-211-24 |
Package Description: | 50 mL in 1 BOTTLE (65649-211-24) |
NDC Code | 65649-211-24 |
Proprietary Name | PEPCID |
Package Description | 50 mL in 1 BOTTLE (65649-211-24) |
Product NDC | 65649-211 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | FAMOTIDINE |
Dosage Form Name | POWDER, FOR SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 19870601 |
Marketing Category Name | NDA |
Labeler Name | Salix Pharmaceuticals, Inc. |
Substance Name | FAMOTIDINE |
Strength Number | 40 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |