Product NDC: | 64980-157 |
Proprietary Name: | Ergocalciferol |
Non Proprietary Name: | Ergocalciferol |
Active Ingredient(s): | 1.25 mg/1 & nbsp; Ergocalciferol |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64980-157 |
Labeler Name: | Rising Pharamceuticals, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA091004 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100723 |
Package NDC: | 64980-157-01 |
Package Description: | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (64980-157-01) |
NDC Code | 64980-157-01 |
Proprietary Name | Ergocalciferol |
Package Description | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (64980-157-01) |
Product NDC | 64980-157 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ergocalciferol |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20100723 |
Marketing Category Name | ANDA |
Labeler Name | Rising Pharamceuticals, Inc |
Substance Name | ERGOCALCIFEROL |
Strength Number | 1.25 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Ergocalciferols [Chemical/Ingredient],Provitamin D2 Compound [EPC] |