Product NDC: | 63717-513 |
Proprietary Name: | Utira-C |
Non Proprietary Name: | Hyoscyamine Sulfate 0.12mg, Methenamine 81.6 mg, Phenyl Salicylate 36.2 mg, Sodium Phosphate Monobasic 40.8 mg, Methylene Blue 10.8 mg |
Active Ingredient(s): | .12; 81.6; 10.8; 36.2; 40.8 mg/1; mg/1; mg/1; mg/1; mg/1 & nbsp; Hyoscyamine Sulfate 0.12mg, Methenamine 81.6 mg, Phenyl Salicylate 36.2 mg, Sodium Phosphate Monobasic 40.8 mg, Methylene Blue 10.8 mg |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, SUGAR COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63717-513 |
Labeler Name: | Hawthorn Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20050901 |
Package NDC: | 63717-513-99 |
Package Description: | 20 BOTTLE in 1 BLISTER PACK (63717-513-99) > 100 TABLET, SUGAR COATED in 1 BOTTLE (63717-513-01) |
NDC Code | 63717-513-99 |
Proprietary Name | Utira-C |
Package Description | 20 BOTTLE in 1 BLISTER PACK (63717-513-99) > 100 TABLET, SUGAR COATED in 1 BOTTLE (63717-513-01) |
Product NDC | 63717-513 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Hyoscyamine Sulfate 0.12mg, Methenamine 81.6 mg, Phenyl Salicylate 36.2 mg, Sodium Phosphate Monobasic 40.8 mg, Methylene Blue 10.8 mg |
Dosage Form Name | TABLET, SUGAR COATED |
Route Name | ORAL |
Start Marketing Date | 20050901 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Hawthorn Pharmaceuticals |
Substance Name | HYOSCYAMINE SULFATE; METHENAMINE; METHYLENE BLUE; PHENYL SALICYLATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE |
Strength Number | .12; 81.6; 10.8; 36.2; 40.8 |
Strength Unit | mg/1; mg/1; mg/1; mg/1; mg/1 |
Pharmaceutical Classes |