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ERGOCALCIFEROL
ERGOCALCIFEROL - 50111-990-01 - (ERGOCALCIFEROL)
Drug Information of ERGOCALCIFEROL
| Product NDC: | 50111-990 |
| 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: | 50111-990 |
| Labeler Name: | Pliva Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA080704 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020601 |
Package Information of ERGOCALCIFEROL
| Package NDC: | 50111-990-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE, PLASTIC (50111-990-01) |
NDC Information of ERGOCALCIFEROL
| NDC Code | 50111-990-01 |
| Proprietary Name | ERGOCALCIFEROL |
| Package Description | 100 CAPSULE in 1 BOTTLE, PLASTIC (50111-990-01) |
| Product NDC | 50111-990 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ERGOCALCIFEROL |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20020601 |
| Marketing Category Name | ANDA |
| Labeler Name | Pliva Inc. |
| Substance Name | ERGOCALCIFEROL |
| Strength Number | 1.25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Ergocalciferols [Chemical/Ingredient],Provitamin D2 Compound [EPC] |
