Home
>
National Drug Code (NDC)
>
Anadrol-50
Anadrol-50 - 68220-055-10 - (oxymetholone)
Drug Information of Anadrol-50
| Product NDC: | 68220-055 |
| Proprietary Name: | Anadrol-50 |
| Non Proprietary Name: | oxymetholone |
| Active Ingredient(s): | 50 mg/1 & nbsp; oxymetholone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Anadrol-50
| Product NDC: | 68220-055 |
| Labeler Name: | Alaven Pharmaceutical |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016848 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19720601 |
Package Information of Anadrol-50
| Package NDC: | 68220-055-10 |
| Package Description: | 1 BOTTLE in 1 CARTON (68220-055-10) > 100 TABLET in 1 BOTTLE |
NDC Information of Anadrol-50
| NDC Code | 68220-055-10 |
| Proprietary Name | Anadrol-50 |
| Package Description | 1 BOTTLE in 1 CARTON (68220-055-10) > 100 TABLET in 1 BOTTLE |
| Product NDC | 68220-055 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | oxymetholone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19720601 |
| Marketing Category Name | NDA |
| Labeler Name | Alaven Pharmaceutical |
| Substance Name | OXYMETHOLONE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
