51079-692 : Bicalutamide 50 mg Oral Tablet


NDC: 51079-692
Labeler: Udl Laboratories, Inc.
Product Type: Human Prescription Drug
Drug Name:  Bicalutamide
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA079185
Rev. Date: 


Appearance:


Markings: M;C17
Shapes:  Round
Colors:  White
Size (mm): 6
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.

M C17: (0378-7017) Bicalutamide 50 mg Oral Tablet by Udl Laboratories, Inc.
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

  • 51079-692-03: 30 BLISTER PACK IN 1 BOX, UNIT‑DOSE (51079‑692‑03) > 1 TABLET, FILM COATED IN 1 BLISTER PACK (51079‑692‑01)

Active Ingredients:

  • Bicalutamide

Dosage Strength:

  • 50 mg

Inactive Ingredients:

  • Silicon Dioxide
  • Hypromelloses
  • Lactose Monohydrate
  • Magnesium Stearate
  • Polydextrose
  • Polyethylene Glycol
  • Povidone
  • Sodium Lauryl Sulfate
  • Sodium Starch Glycolate Type a Potato
  • Titanium Dioxide
  • Triacetin

Pharmaceutical Classes:

  • Androgen Receptor Antagonists [MoA]
  • Androgen Receptor Inhibitor [EPC]

Related Products:

Based on records with the same trade name.
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NDC 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.