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Zemplar
Zemplar - 0074-4317-72 - (Paricalcitol)
Drug Information of Zemplar
| Product NDC: | 0074-4317 |
| Proprietary Name: | Zemplar |
| Non Proprietary Name: | Paricalcitol |
| Active Ingredient(s): | 1 ug/1 & nbsp; Paricalcitol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zemplar
| Product NDC: | 0074-4317 |
| Labeler Name: | AbbVie Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021606 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100614 |
Package Information of Zemplar
| Package NDC: | 0074-4317-72 |
| Package Description: | 1 BOTTLE in 1 CARTON (0074-4317-72) > 7 CAPSULE, LIQUID FILLED in 1 BOTTLE |
NDC Information of Zemplar
| NDC Code | 0074-4317-72 |
| Proprietary Name | Zemplar |
| Package Description | 1 BOTTLE in 1 CARTON (0074-4317-72) > 7 CAPSULE, LIQUID FILLED in 1 BOTTLE |
| Product NDC | 0074-4317 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Paricalcitol |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20100614 |
| Marketing Category Name | NDA |
| Labeler Name | AbbVie Inc. |
| Substance Name | PARICALCITOL |
| Strength Number | 1 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC] |
