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Urelle
Urelle - 66663-219-01 - (hyoscyamine sulfate, methenamine, methylene blue, phenyl salicylate, and sodium phosphate, monobasic, monohydrate)
Drug Information of Urelle
| Product NDC: | 66663-219 |
| Proprietary Name: | Urelle |
| Non Proprietary Name: | hyoscyamine sulfate, methenamine, methylene blue, phenyl salicylate, and sodium phosphate, monobasic, monohydrate |
| Active Ingredient(s): | .12; 81; 10.8; 32.4; 40.8 mg/1; mg/1; mg/1; mg/1; mg/1 & nbsp; hyoscyamine sulfate, methenamine, methylene blue, phenyl salicylate, and sodium phosphate, monobasic, monohydrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Urelle
| Product NDC: | 66663-219 |
| Labeler Name: | Jazz Pharmaceuticals Commercial Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20020101 |
Package Information of Urelle
| Package NDC: | 66663-219-01 |
| Package Description: | 90 TABLET in 1 BOTTLE (66663-219-01) |
NDC Information of Urelle
| NDC Code | 66663-219-01 |
| Proprietary Name | Urelle |
| Package Description | 90 TABLET in 1 BOTTLE (66663-219-01) |
| Product NDC | 66663-219 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hyoscyamine sulfate, methenamine, methylene blue, phenyl salicylate, and sodium phosphate, monobasic, monohydrate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20020101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Jazz Pharmaceuticals Commercial Corp. |
| Substance Name | HYOSCYAMINE SULFATE; METHENAMINE; METHYLENE BLUE; PHENYL SALICYLATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE |
| Strength Number | .12; 81; 10.8; 32.4; 40.8 |
| Strength Unit | mg/1; mg/1; mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
