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Methenamine Mandelate
Methenamine Mandelate - 13925-107-01 - (Methenamine Mandelate)
Drug Information of Methenamine Mandelate
| Product NDC: | 13925-107 |
| Proprietary Name: | Methenamine Mandelate |
| Non Proprietary Name: | Methenamine Mandelate |
| Active Ingredient(s): | 1000 mg/1 & nbsp; Methenamine Mandelate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Methenamine Mandelate
| Product NDC: | 13925-107 |
| Labeler Name: | Seton Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100201 |
Package Information of Methenamine Mandelate
| Package NDC: | 13925-107-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (13925-107-01) |
NDC Information of Methenamine Mandelate
| NDC Code | 13925-107-01 |
| Proprietary Name | Methenamine Mandelate |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (13925-107-01) |
| Product NDC | 13925-107 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Methenamine Mandelate |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100201 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Seton Pharmaceuticals |
| Substance Name | METHENAMINE MANDELATE |
| Strength Number | 1000 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
