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Cytra-K Cystrals
Cytra-K Cystrals - 60258-005-01 - (Potassium Citrate and Citric Acid)
Drug Information of Cytra-K Cystrals
| Product NDC: | 60258-005 |
| Proprietary Name: | Cytra-K Cystrals |
| Non Proprietary Name: | Potassium Citrate and Citric Acid |
| Active Ingredient(s): | 1.002; 3.3 g/1; g/1 & nbsp; Potassium Citrate and Citric Acid |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GRANULE, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cytra-K Cystrals
| Product NDC: | 60258-005 |
| Labeler Name: | Cypress Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20030501 |
Package Information of Cytra-K Cystrals
| Package NDC: | 60258-005-01 |
| Package Description: | 100 GRANULE, FOR SOLUTION in 1 BOX (60258-005-01) |
NDC Information of Cytra-K Cystrals
| NDC Code | 60258-005-01 |
| Proprietary Name | Cytra-K Cystrals |
| Package Description | 100 GRANULE, FOR SOLUTION in 1 BOX (60258-005-01) |
| Product NDC | 60258-005 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Potassium Citrate and Citric Acid |
| Dosage Form Name | GRANULE, FOR SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20030501 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Cypress Pharmaceutical, Inc. |
| Substance Name | CITRIC ACID MONOHYDRATE; POTASSIUM CITRATE |
| Strength Number | 1.002; 3.3 |
| Strength Unit | g/1; g/1 |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
