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oxandrolone
oxandrolone - 0591-3544-01 - (oxandrolone)
Drug Information of oxandrolone
| Product NDC: | 0591-3544 |
| Proprietary Name: | oxandrolone |
| Non Proprietary Name: | oxandrolone |
| Active Ingredient(s): | 2.5 mg/1 & nbsp; oxandrolone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of oxandrolone
| Product NDC: | 0591-3544 |
| Labeler Name: | Watson Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA013718 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20070101 |
Package Information of oxandrolone
| Package NDC: | 0591-3544-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (0591-3544-01) |
NDC Information of oxandrolone
| NDC Code | 0591-3544-01 |
| Proprietary Name | oxandrolone |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0591-3544-01) |
| Product NDC | 0591-3544 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | oxandrolone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070101 |
| Marketing Category Name | NDA |
| Labeler Name | Watson Laboratories, Inc. |
| Substance Name | OXANDROLONE |
| Strength Number | 2.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
