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Oxandrolone
Oxandrolone - 49884-301-01 - (oxandrolone)
Drug Information of Oxandrolone
| Product NDC: | 49884-301 |
| 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: | 49884-301 |
| Labeler Name: | Par Pharmaceutical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077827 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070820 |
Package Information of Oxandrolone
| Package NDC: | 49884-301-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (49884-301-01) |
NDC Information of Oxandrolone
| NDC Code | 49884-301-01 |
| Proprietary Name | Oxandrolone |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (49884-301-01) |
| Product NDC | 49884-301 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | oxandrolone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070820 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical Inc. |
| Substance Name | OXANDROLONE |
| Strength Number | 2.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
