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Vitamin D
Vitamin D - 0574-0194-50 - (ERGOCALCIFEROL)
Drug Information of Vitamin D
| 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) |
Labeler Information of Vitamin D
| 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 Information of Vitamin D
| Package NDC: | 0574-0194-50 |
| Package Description: | 50 CAPSULE in 1 BOTTLE, GLASS (0574-0194-50) |
NDC Information of Vitamin D
| NDC Code | 0574-0194-50 |
| Proprietary Name | Vitamin D |
| Package Description | 50 CAPSULE in 1 BOTTLE, GLASS (0574-0194-50) |
| 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] |
