NDC 49884-301

Oxandrolone

Oxandrolone

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.

• Product ID: 49884-301_bb9cafda-1f4b-46ec-bf77-710def6c70de
• NDC: 49884-301
• 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: Par Pharmaceutical, Inc.
• Substance Name: OXANDROLONE
• Active Ingredient Strength: 3 mg/1
• DEA Schedule: CIII
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 49884-301-01

100 TABLET in 1 BOTTLE, PLASTIC (49884-301-01)

• Marketing Start Date: 2007-08-20
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 49884-301-01 [49884030101]

Oxandrolone TABLET

• Marketing Category: ANDA
• Application Number: ANDA077827
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2007-08-20

Drug Details

Active Ingredients

Ingredient	Strength
OXANDROLONE	2.5 mg/1

OpenFDA Data

• SPL SET ID: a6f42739-5bfc-4b76-8795-e93fa58f3d29
• Manufacturer:
  • Par Pharmaceutical, Inc.
• UNII:
  • 7H6TM3CT4L
• RxNorm Concept Unique ID - RxCUI:
  • 351276
  • 198056

Medicade Reported Pricing

49884030101 OXANDROLONE 2.5 MG TABLET

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "Oxandrolone" or generic name "Oxandrolone"

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