oxandrolone is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Upsher-smith Laboratories, Llc. The primary component is Oxandrolone.
Product ID | 0245-0272_07d23eea-3550-4eae-a5f2-557a81c1fd6f |
NDC | 0245-0272 |
Product Type | Human Prescription Drug |
Proprietary Name | oxandrolone |
Generic Name | Oxandrolone |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2007-03-22 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA078033 |
Labeler Name | Upsher-Smith Laboratories, LLC |
Substance Name | OXANDROLONE |
Active Ingredient Strength | 10 mg/1 |
DEA Schedule | CIII |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |
Marketing Start Date | 2007-03-22 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA078033 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-03-22 |
Marketing Category | ANDA |
Application Number | ANDA078033 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2007-03-22 |
Marketing Category | ANDA |
Application Number | ANDA078033 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2007-03-22 |
Marketing Category | ANDA |
Application Number | ANDA078033 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2007-03-22 |
Ingredient | Strength |
---|---|
OXANDROLONE | 10 mg/1 |
SPL SET ID: | 8e6af85f-e44e-4c47-8a1a-7c5cb7893167 |
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 |