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Calcitriol
Calcitriol - 63323-731-01 - (CALCITRIOL)
Drug Information of Calcitriol
| Product NDC: | 63323-731 |
| Proprietary Name: | Calcitriol |
| Non Proprietary Name: | CALCITRIOL |
| Active Ingredient(s): | 1 ug/mL & nbsp; CALCITRIOL |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Calcitriol
| Product NDC: | 63323-731 |
| Labeler Name: | Fresenius Kabi USA, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075836 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030529 |
Package Information of Calcitriol
| Package NDC: | 63323-731-01 |
| Package Description: | 5 TRAY in 1 CARTON (63323-731-01) > 10 AMPULE in 1 TRAY > 1 mL in 1 AMPULE |
NDC Information of Calcitriol
| NDC Code | 63323-731-01 |
| Proprietary Name | Calcitriol |
| Package Description | 5 TRAY in 1 CARTON (63323-731-01) > 10 AMPULE in 1 TRAY > 1 mL in 1 AMPULE |
| Product NDC | 63323-731 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CALCITRIOL |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20030529 |
| Marketing Category Name | ANDA |
| Labeler Name | Fresenius Kabi USA, LLC |
| Substance Name | CALCITRIOL |
| Strength Number | 1 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes | Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC] |
