80725-620 : Myleran 2 mg Oral Tablet, Film Coated


NDC: 80725-620
Labeler: Waylis Therapeutics LLC
Product Type: Human Prescription Drug
Drug Name:  Myleran
Dosage Form: Oral Tablet, Film Coated
Application #: NDA009386
Rev. Date: 


NDC Package Codes:

  • 80725-620-25: 25 TABLET, FILM COATED IN 1 BOTTLE (80725‑620‑25)

Active Ingredients:

  • Busulfan

Dosage Strength:

  • 2 mg

Pharmaceutical Classes:

  • Alkylating Activity [MoA]
  • Alkylating Drug [EPC]

Related Products:

Based on records with the same trade name.
  • 0173-0713 Myleran 2 mg Oral Tablet by Glaxosmithkline LLC
  • 69784-620 Myleran 2 mg Oral Tablet, Film Coated by Woodward Pharma Services LLC
  • 76388-713 Myleran 2 mg Oral Tablet by Aspen Global Inc.

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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.