Product NDC: | 52125-085 |
Proprietary Name: | Hectorol |
Non Proprietary Name: | doxercalciferol |
Active Ingredient(s): | .5 ug/1 & nbsp; doxercalciferol |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52125-085 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020862 |
Marketing Category: | NDA |
Start Marketing Date: | 20120920 |
Package NDC: | 52125-085-02 |
Package Description: | 30 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (52125-085-02) |
NDC Code | 52125-085-02 |
Proprietary Name | Hectorol |
Package Description | 30 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (52125-085-02) |
Product NDC | 52125-085 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | doxercalciferol |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20120920 |
Marketing Category Name | NDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | DOXERCALCIFEROL |
Strength Number | .5 |
Strength Unit | ug/1 |
Pharmaceutical Classes | Ergocalciferols [Chemical/Ingredient],Vitamin D2 Analog [EPC] |