Methenamine Mandelate is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Edenbridge Pharmaceuticals Llc.. The primary component is Methenamine Mandelate.
| Product ID | 42799-106_42dda043-7e70-4fcd-9fcc-96f70d751efa |
| NDC | 42799-106 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Methenamine Mandelate |
| Generic Name | Methenamine Mandelate |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2009-12-15 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | Edenbridge Pharmaceuticals LLC. |
| Substance Name | METHENAMINE MANDELATE |
| Active Ingredient Strength | 1000 mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |
| Marketing Start Date | 2009-12-15 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-12-15 |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2009-12-15 |
| Ingredient | Strength |
|---|---|
| METHENAMINE MANDELATE | 1000 mg/1 |
| SPL SET ID: | cc299e8a-cf9a-4dc6-b6e6-972141e59296 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 13925-107 | Methenamine Mandelate | Methenamine Mandelate |
| 42799-105 | Methenamine Mandelate | Methenamine Mandelate |
| 42799-106 | Methenamine Mandelate | Methenamine Mandelate |
| 58657-460 | Methenamine Mandelate | Methenamine Mandelate |
| 62135-200 | Methenamine Mandelate | Methenamine Mandelate |
| 62135-201 | Methenamine Mandelate | Methenamine Mandelate |
| 63629-1147 | Methenamine Mandelate | Methenamine Mandelate |