Product NDC: | 60258-001 |
Proprietary Name: | Cytra-2 |
Non Proprietary Name: | Sodium Citrate and Citric Acid |
Active Ingredient(s): | 334; 500 mg/5mL; mg/5mL & nbsp; Sodium Citrate and Citric Acid |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60258-001 |
Labeler Name: | Cypress Pharmaceutical, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20081001 |
Package NDC: | 60258-001-16 |
Package Description: | 473 mL in 1 BOTTLE, PLASTIC (60258-001-16) |
NDC Code | 60258-001-16 |
Proprietary Name | Cytra-2 |
Package Description | 473 mL in 1 BOTTLE, PLASTIC (60258-001-16) |
Product NDC | 60258-001 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sodium Citrate and Citric Acid |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20081001 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Cypress Pharmaceutical, Inc. |
Substance Name | CITRIC ACID MONOHYDRATE; TRISODIUM CITRATE DIHYDRATE |
Strength Number | 334; 500 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes |