69539-049 : Abiraterone 250 mg Oral Tablet


NDC: 69539-049
Labeler: Msn Laboratories Private Limited
Product Type: Human Prescription Drug
Drug Name:  Abiraterone
Dosage Form: Oral Tablet
Application #: ANDA210686
Rev. Date: 


Appearance:


Markings: ABR;250
Shapes:  Oval
Colors:  White
Size (mm): 16
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

  • 69539-049-92: 120 TABLET IN 1 BOTTLE (69539‑049‑92)

Active Ingredients:

  • Abiraterone Acetate

Dosage Strength:

  • 250 mg

Inactive Ingredients:

  • Silicon Dioxide
  • Croscarmellose Sodium
  • Lactose Monohydrate
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Povidone
  • Sodium Lauryl Sulfate /

Pharmaceutical Classes:

  • Cytochrome P450 17A1 Inhibitor [EPC]
  • Cytochrome P450 17A1 Inhibitors [MoA]
  • Cytochrome P450 2C8 Inhibitors [MoA]
  • Cytochrome P450 2D6 Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 0143-9597 Abiraterone 250 mg Oral Tablet by West-ward Pharmaceuticals Corp
  • 68001-489 Abiraterone 250 mg Oral Tablet by Bluepoint Laboratories
  • 72205-030 Abiraterone 250 mg Oral Tablet by Novadoz Pharmaceuticals LLC
  • 72789-213 Abiraterone 250 mg Oral Tablet by Pd-rx Pharmaceuticals, Inc.
  • 82249-010 Abiraterone 250 mg Oral; Oral Tablet by Civicascript, LLC

NDC QR Code

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NDC 69539-049 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.