0517-0920 : N/A 6 mg/ml Intravenous Injection


NDC: 0517-0920
Labeler: American Regent, Inc.
Product Type: Human Prescription Drug
Drug Name:  N/A
Dosage Form: Intravenous Injection
Application #: ANDA202259
Rev. Date: 


NDC Package Codes:

  • 0517-0920-08: 8 VIAL IN 1 PACKAGE (0517‑0920‑08) > 10 ML IN 1 VIAL (0517‑0920‑01)

Active Ingredients:

  • Busulfan

Dosage Strength:

  • 6 mg/mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 0054-9628 N/A .5 g/ml Oral Solution by Hikma Pharmaceuticals USA Inc.
  • 43386-405 N/A 500 mg Oral Tablet by Lupin Pharmaceuticals, Inc.
  • 71053-590 N/A .5 mg/.7ml Intramuscular Injection by Rafa Laboratories, Ltd.
  • 71053-591 N/A 1 mg/.7ml Intramuscular Injection by Rafa Laboratories, Ltd.
  • 71053-592 N/A 2 mg/.7ml Intramuscular Injection by Rafa Laboratories, Ltd.
  • 71053-595 N/A 10 mg/.7ml Intramuscular Injection, Solution by Rafa Laboratories, Ltd.

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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.