24338-342 : Gleostine 100 mg Oral Capsule, Gelatin Coated


NDC: 24338-342
Labeler: Azurity Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Drug Name:  Gleostine
Dosage Form: Oral Capsule, Gelatin Coated
Application #: NDA017588
Rev. Date: 


NDC Package Codes:

  • 24338-342-05: 1 BOTTLE IN 1 CARTON (24338‑342‑05) / 5 CAPSULE, GELATIN COATED IN 1 BOTTLE

Active Ingredients:

  • Lomustine

Dosage Strength:

  • 100 mg

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 24338-340 Gleostine 10 mg Oral Capsule, Gelatin Coated by Azurity Pharmaceuticals, Inc.
  • 24338-341 Gleostine 40 mg Oral Capsule, Gelatin Coated by Azurity Pharmaceuticals, Inc.
  • 58181-3040 Gleostine 10 mg Oral Capsule, Gelatin Coated by Nextsource Biotechnology, LLC
  • 58181-3041 Gleostine 40 mg Oral Capsule, Gelatin Coated by Nextsource Biotechnology, LLC
  • 58181-3042 Gleostine 100 mg Oral Capsule, Gelatin Coated by Nextsource Biotechnology, LLC
  • 58181-3043 Gleostine 5 mg Oral Capsule, Gelatin Coated by Nextsource Biotechnology, LLC

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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.