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Ergocalciferol
Ergocalciferol - 51991-604-01 - (Ergocalciferol)
Drug Information of Ergocalciferol
| Product NDC: | 51991-604 |
| Proprietary Name: | Ergocalciferol |
| 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) |
Labeler Information of Ergocalciferol
| Product NDC: | 51991-604 |
| Labeler Name: | Breckenridge Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040833 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090817 |
Package Information of Ergocalciferol
| Package NDC: | 51991-604-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE, PLASTIC (51991-604-01) |
NDC Information of Ergocalciferol
| NDC Code | 51991-604-01 |
| Proprietary Name | Ergocalciferol |
| Package Description | 100 CAPSULE in 1 BOTTLE, PLASTIC (51991-604-01) |
| Product NDC | 51991-604 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ergocalciferol |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20090817 |
| Marketing Category Name | ANDA |
| Labeler Name | Breckenridge Pharmaceutical, Inc. |
| Substance Name | ERGOCALCIFEROL |
| Strength Number | 1.25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Ergocalciferols [Chemical/Ingredient],Provitamin D2 Compound [EPC] |
