| Product NDC: | 66336-907 | 
| 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) | 
| Product NDC: | 66336-907 | 
| Labeler Name: | Dispensing Solutions, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA040833 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20090817 | 
| Package NDC: | 66336-907-44 | 
| Package Description: | 4 CAPSULE in 1 BOTTLE (66336-907-44) | 
| NDC Code | 66336-907-44 | 
| Proprietary Name | Ergocalciferol | 
| Package Description | 4 CAPSULE in 1 BOTTLE (66336-907-44) | 
| Product NDC | 66336-907 | 
| 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 | Dispensing Solutions, Inc. | 
| Substance Name | ERGOCALCIFEROL | 
| Strength Number | 1.25 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes | Ergocalciferols [Chemical/Ingredient],Provitamin D2 Compound [EPC] |