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CYTRA
CYTRA - 60258-002-16 - (Potassium Citrate Monohydrate, Sodium Citrate Dihydrate, Citric Acid Monohydrate)
Drug Information of CYTRA
| Product NDC: | 60258-002 |
| Proprietary Name: | CYTRA |
| Non Proprietary Name: | Potassium Citrate Monohydrate, Sodium Citrate Dihydrate, Citric Acid Monohydrate |
| Active Ingredient(s): | 334; 550; 500 mg/5mL; mg/5mL; mg/5mL & nbsp; Potassium Citrate Monohydrate, Sodium Citrate Dihydrate, Citric Acid Monohydrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CYTRA
| Product NDC: | 60258-002 |
| Labeler Name: | Cypress Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20080729 |
Package Information of CYTRA
| Package NDC: | 60258-002-16 |
| Package Description: | 473 mL in 1 BOTTLE (60258-002-16) |
NDC Information of CYTRA
| NDC Code | 60258-002-16 |
| Proprietary Name | CYTRA |
| Package Description | 473 mL in 1 BOTTLE (60258-002-16) |
| Product NDC | 60258-002 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Potassium Citrate Monohydrate, Sodium Citrate Dihydrate, Citric Acid Monohydrate |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20080729 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Cypress Pharmaceuticals, Inc |
| Substance Name | CITRIC ACID MONOHYDRATE; POTASSIUM CITRATE; SODIUM CITRATE |
| Strength Number | 334; 550; 500 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
