Product NDC: | 42998-649 |
Proprietary Name: | Pepcid |
Non Proprietary Name: | famotidine |
Active Ingredient(s): | 40 mg/1 & nbsp; famotidine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42998-649 |
Labeler Name: | Marathon Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019462 |
Marketing Category: | NDA |
Start Marketing Date: | 19861015 |
Package NDC: | 42998-649-09 |
Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (42998-649-09) |
NDC Code | 42998-649-09 |
Proprietary Name | Pepcid |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (42998-649-09) |
Product NDC | 42998-649 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | famotidine |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 19861015 |
Marketing Category Name | NDA |
Labeler Name | Marathon Pharmaceuticals, LLC |
Substance Name | FAMOTIDINE |
Strength Number | 40 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |