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NDC 49884-0301-01 Oxandrolone 2.5 mg/1 Details
Oxandrolone 2.5 mg/1
Oxandrolone is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Par Pharmaceutical, Inc.. The primary component is OXANDROLONE.
MedlinePlus Drug Summary
Oxandrolone is used with a diet program to cause weight gain in people who have lost too much weight due to surgery, injury, chronic (long-lasting) infections, trauma, or who are underweight for unknown reasons. Oxandrolone is also used to treat bone pain in people with osteoporosis (a condition in which the bones become thin and weak and break easily) and to prevent certain side effects in people who take corticosteroids (a group of medications used to treat many conditions that involve inflammation or swelling of part of the body) for a long time. Oxandrolone is in a class of medications called androgenic hormones. It works by increasing the amount of protein made by the body. This protein is used to build more muscle and increase body weight.
Related Packages: 49884-0301-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Oxandrolone
Product Information
| NDC | 49884-0301 |
|---|---|
| Product ID | 49884-301_44c3143a-50c5-4951-83cb-9a0a1bcc0802 |
| Associated GPIs | 23200040000305 |
| GCN Sequence Number | 003180 |
| GCN Sequence Number Description | oxandrolone TABLET 2.5 MG ORAL |
| HIC3 | F1A |
| HIC3 Description | ANDROGENIC AGENTS |
| GCN | 10561 |
| HICL Sequence Number | 001412 |
| HICL Sequence Number Description | OXANDROLONE |
| Brand/Generic | Generic |
| Proprietary Name | Oxandrolone |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | oxandrolone |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 2.5 |
| Active Ingredient Units | mg/1 |
| Substance Name | OXANDROLONE |
| Labeler Name | Par Pharmaceutical, Inc. |
| Pharmaceutical Class | n/a |
| DEA Schedule | CIII |
| Marketing Category | ANDA |
| Application Number | ANDA077827 |
| Listing Certified Through | n/a |
Package
NDC 49884-0301-01 (49884030101)
| NDC Package Code | 49884-301-01 |
|---|---|
| Billing NDC | 49884030101 |
| Package | 100 TABLET in 1 BOTTLE, PLASTIC (49884-301-01) |
| Marketing Start Date | 2007-08-20 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |