Oxandrolone is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by American Health Packaging. The primary component is Oxandrolone.
| Product ID | 68084-425_82ce9e1d-3287-cacf-e053-2a91aa0ae1ad |
| NDC | 68084-425 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Oxandrolone |
| Generic Name | Oxandrolone |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2015-12-09 |
| Marketing End Date | 2020-03-31 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA077827 |
| Labeler Name | American Health Packaging |
| Substance Name | OXANDROLONE |
| Active Ingredient Strength | 10 mg/1 |
| DEA Schedule | CIII |
| NDC Exclude Flag | N |
| Marketing Start Date | 2015-12-09 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA077827 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-12-09 |
| Marketing End Date | 2020-03-31 |
| Marketing Category | ANDA |
| Application Number | ANDA077827 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-12-09 |
| Marketing End Date | 2020-03-31 |
| Ingredient | Strength |
|---|---|
| OXANDROLONE | 10 mg/1 |
| SPL SET ID: | b3d24364-f4fc-4aac-ac5c-651ae7f6f9b6 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0245-0271 | Oxandrolone | Oxandrolone |
| 0245-0272 | oxandrolone | oxandrolone |
| 49884-301 | Oxandrolone | oxandrolone |
| 49884-302 | Oxandrolone | oxandrolone |
| 63629-7603 | Oxandrolone | oxandrolone |
| 68084-424 | Oxandrolone | oxandrolone |
| 68084-425 | Oxandrolone | oxandrolone |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() OXANDROLONE 85354270 4126968 Live/Registered |
PBB TRADEMARK HOLDINGS, LLC 2011-06-23 |