Oxandrolone is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Oxandrolone.
Product ID | 63629-7603_3e01cc2f-dd9b-4055-8fe1-2b87d22800d4 |
NDC | 63629-7603 |
Product Type | Human Prescription Drug |
Proprietary Name | Oxandrolone |
Generic Name | Oxandrolone |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2007-08-20 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA077827 |
Labeler Name | Bryant Ranch Prepack |
Substance Name | OXANDROLONE |
Active Ingredient Strength | 3 mg/1 |
DEA Schedule | CIII |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |
Marketing Start Date | 2022-04-29 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA077827 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-05-09 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA077827 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-05-09 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA077827 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-05-09 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
OXANDROLONE | 2.5 mg/1 |
SPL SET ID: | 7127ac16-f673-4b66-b5e5-5f881c85aa39 |
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 |