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oxandrolone
oxandrolone - 0245-0272-06 - (oxandrolone)
Drug Information of oxandrolone
| Product NDC: | 0245-0272 |
| Proprietary Name: | oxandrolone |
| Non Proprietary Name: | oxandrolone |
| Active Ingredient(s): | 10 mg/1 & nbsp; oxandrolone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of oxandrolone
| Product NDC: | 0245-0272 |
| Labeler Name: | Upsher-Smith Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078033 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070322 |
Package Information of oxandrolone
| Package NDC: | 0245-0272-06 |
| Package Description: | 60 TABLET in 1 BOTTLE (0245-0272-06) |
NDC Information of oxandrolone
| NDC Code | 0245-0272-06 |
| Proprietary Name | oxandrolone |
| Package Description | 60 TABLET in 1 BOTTLE (0245-0272-06) |
| Product NDC | 0245-0272 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | oxandrolone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070322 |
| Marketing Category Name | ANDA |
| Labeler Name | Upsher-Smith Laboratories, Inc. |
| Substance Name | OXANDROLONE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
