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Cytra-K
Cytra-K - 60258-003-16 - (Potassium Citrate and Citric Acid)
Drug Information of Cytra-K
| Product NDC: | 60258-003 |
| Proprietary Name: | Cytra-K |
| Non Proprietary Name: | Potassium Citrate and Citric Acid |
| Active Ingredient(s): | 334; 1100 mg/5mL; mg/5mL & nbsp; Potassium Citrate and Citric Acid |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cytra-K
| Product NDC: | 60258-003 |
| Labeler Name: | Cypress Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20080930 |
Package Information of Cytra-K
| Package NDC: | 60258-003-16 |
| Package Description: | 473 mL in 1 BOTTLE, PLASTIC (60258-003-16) |
NDC Information of Cytra-K
| NDC Code | 60258-003-16 |
| Proprietary Name | Cytra-K |
| Package Description | 473 mL in 1 BOTTLE, PLASTIC (60258-003-16) |
| Product NDC | 60258-003 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Potassium Citrate and Citric Acid |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20080930 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Cypress Pharmaceutical, Inc. |
| Substance Name | CITRIC ACID MONOHYDRATE; POTASSIUM CITRATE |
| Strength Number | 334; 1100 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
