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Cyclophosphamide
Cyclophosphamide - 54868-5005-0 - (Cyclophosphamide)
Drug Information of Cyclophosphamide
| Product NDC: | 54868-5005 |
| Proprietary Name: | Cyclophosphamide |
| Non Proprietary Name: | Cyclophosphamide |
| Active Ingredient(s): | 50 mg/1 & nbsp; Cyclophosphamide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cyclophosphamide
| Product NDC: | 54868-5005 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040032 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19990817 |
Package Information of Cyclophosphamide
| Package NDC: | 54868-5005-0 |
| Package Description: | 100 TABLET in 1 BOTTLE (54868-5005-0) |
NDC Information of Cyclophosphamide
| NDC Code | 54868-5005-0 |
| Proprietary Name | Cyclophosphamide |
| Package Description | 100 TABLET in 1 BOTTLE (54868-5005-0) |
| Product NDC | 54868-5005 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cyclophosphamide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19990817 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | CYCLOPHOSPHAMIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
