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Calcitriol
Calcitriol - 0093-0658-01 - (Calcitriol)
Drug Information of Calcitriol
| Product NDC: | 0093-0658 |
| Proprietary Name: | Calcitriol |
| Non Proprietary Name: | Calcitriol |
| Active Ingredient(s): | .5 ug/1 & nbsp; Calcitriol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Calcitriol
| Product NDC: | 0093-0658 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075765 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20011015 |
Package Information of Calcitriol
| Package NDC: | 0093-0658-01 |
| Package Description: | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (0093-0658-01) |
NDC Information of Calcitriol
| NDC Code | 0093-0658-01 |
| Proprietary Name | Calcitriol |
| Package Description | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (0093-0658-01) |
| Product NDC | 0093-0658 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Calcitriol |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20011015 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | CALCITRIOL |
| Strength Number | .5 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC] |
