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Ergocalciferol
Ergocalciferol - 42291-274-50 - (Ergocalciferol)
Drug Information of Ergocalciferol
| Product NDC: | 42291-274 |
| 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) |
Labeler Information of Ergocalciferol
| Product NDC: | 42291-274 |
| Labeler Name: | AvKARE, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091004 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120605 |
Package Information of Ergocalciferol
| Package NDC: | 42291-274-50 |
| Package Description: | 500 CAPSULE, LIQUID FILLED in 1 BOTTLE (42291-274-50) |
NDC Information of Ergocalciferol
| NDC Code | 42291-274-50 |
| Proprietary Name | Ergocalciferol |
| Package Description | 500 CAPSULE, LIQUID FILLED in 1 BOTTLE (42291-274-50) |
| Product NDC | 42291-274 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ergocalciferol |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20120605 |
| Marketing Category Name | ANDA |
| Labeler Name | AvKARE, Inc. |
| Substance Name | ERGOCALCIFEROL |
| Strength Number | 1.25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Ergocalciferols [Chemical/Ingredient],Provitamin D2 Compound [EPC] |
