Product NDC: | 0574-0194 |
Proprietary Name: | Vitamin D |
Non Proprietary Name: | ERGOCALCIFEROL |
Active Ingredient(s): | 1.25 mg/1 & nbsp; ERGOCALCIFEROL |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0574-0194 |
Labeler Name: | Paddock Laboratories, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090455 |
Marketing Category: | ANDA |
Start Marketing Date: | 20091215 |
Package NDC: | 0574-0194-51 |
Package Description: | 100 CAPSULE in 1 BOTTLE, PLASTIC (0574-0194-51) |
NDC Code | 0574-0194-51 |
Proprietary Name | Vitamin D |
Package Description | 100 CAPSULE in 1 BOTTLE, PLASTIC (0574-0194-51) |
Product NDC | 0574-0194 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ERGOCALCIFEROL |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20091215 |
Marketing Category Name | ANDA |
Labeler Name | Paddock Laboratories, LLC |
Substance Name | ERGOCALCIFEROL |
Strength Number | 1.25 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Ergocalciferols [Chemical/Ingredient],Provitamin D2 Compound [EPC] |