| Product NDC: | 0024-0392 |
| Proprietary Name: | Drisdol |
| 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: | 0024-0392 |
| Labeler Name: | sanofi-aventis U.S. LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA003444 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19741111 |
| Package NDC: | 0024-0392-02 |
| Package Description: | 50 CAPSULE in 1 BOTTLE, GLASS (0024-0392-02) |
| NDC Code | 0024-0392-02 |
| Proprietary Name | Drisdol |
| Package Description | 50 CAPSULE in 1 BOTTLE, GLASS (0024-0392-02) |
| Product NDC | 0024-0392 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ergocalciferol |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19741111 |
| Marketing Category Name | NDA |
| Labeler Name | sanofi-aventis U.S. LLC |
| Substance Name | ERGOCALCIFEROL |
| Strength Number | 1.25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Ergocalciferols [Chemical/Ingredient],Provitamin D2 Compound [EPC] |