0548-5001 : Ganirelix Acetate 250 ug/.5ml Subcutaneous Injection


NDC0548-5001
Labeler: Amphastar Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Drug Name:  Ganirelix Acetate
Dosage Form: Subcutaneous Injection
Application #: ANDA212613
Rev. Date: 


NDC Package Codes:

  • 0548-5001-00: 1 SYRINGE IN 1 CARTON (0548‑5001‑00) > .5 ML IN 1 SYRINGE

Active Ingredients:

  • Ganirelix Acetate

Dosage Strength:

  • 250 ug/.5mL

Pharmaceutical Classes:

  • Decreased GnRH Secretion [PE]
  • Gonadotropin Releasing Hormone Receptor Antagonist [EPC]
  • Gonadotropin Releasing Hormone Receptor Antagonists [MoA]

Related Products:

Based on records with the same trade name.
  • 0052-0301 Ganirelix Acetate 250 ug/.5ml Subcutaneous Injection, Solution by Organon USA Inc.
  • 55566-1000 Ganirelix Acetate 250 ug/.5ml Subcutaneous Injection, Solution by Ferring Pharmaceuticals Inc.
  • 65219-028 Ganirelix Acetate 250 ug/.5ml Subcutaneous Injection by Fresenius Kabi USA, LLC
  • 68083-472 Ganirelix Acetate 250 ug/.5ml Subcutaneous Injection, Solution by Gland Pharma Limited
  • 70748-274 Ganirelix Acetate 250 ug/.5ml Subcutaneous Injection, Solution by Lupin Pharmaceuticals, Inc.
  • 71288-554 Ganirelix Acetate 250 ug/.5ml Subcutaneous Injection, Solution by Meitheal Pharmaceuticals Inc.
  • 78206-138 Ganirelix Acetate 250 ug/.5ml Subcutaneous Injection, Solution by Organon LLC

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.