69605-810 : Reditrex 10 mg/.4ml Subcutaneous Injection, Solution


NDC: 69605-810
Labeler: Cenexi - Bla
Product Type: Human Prescription Drug
Drug Name:  Reditrex
Dosage Form: Subcutaneous Injection, Solution
Application #: NDA210737
Rev. Date: 


NDC Package Codes:

  • 69605-810-22: 4 CARTON IN 1 CASE (69605‑810‑22) > 1 SYRINGE IN 1 CARTON (69605‑810‑11) > .4 ML IN 1 SYRINGE

Active Ingredients:

  • Methotrexate

Dosage Strength:

  • 10 mg/.4mL

Pharmaceutical Classes:

  • Folate Analog Metabolic Inhibitor [EPC]
  • Folic Acid Metabolism Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 69605-807 Reditrex 7.5 mg/.3ml Subcutaneous Injection, Solution by Cenexi - Bla
  • 69605-812 Reditrex 12.5 mg/.5ml Subcutaneous Injection, Solution by Cenexi - Bla
  • 69605-815 Reditrex 15 mg/.6ml Subcutaneous Injection, Solution by Cenexi - Bla
  • 69605-817 Reditrex 17.5 mg/.7ml Subcutaneous Injection, Solution by Cenexi - Bla
  • 69605-820 Reditrex 20 mg/.8ml Subcutaneous Injection, Solution by Cenexi - Bla
  • 69605-822 Reditrex 22.5 mg/.9ml Subcutaneous Injection, Solution by Cenexi - Bla
  • 69605-825 Reditrex 25 mg/ml Subcutaneous Injection, Solution by Cenexi - Bla
  • 66220-807 Reditrex 7.5 mg/.3ml Subcutaneous Injection, Solution by Cumberland Pharmaceuticals Inc.
  • 66220-810 Reditrex 10 mg/.4ml Subcutaneous Injection, Solution by Cumberland Pharmaceuticals Inc.
  • 66220-812 Reditrex 12.5 mg/.5ml Subcutaneous Injection, Solution by Cumberland Pharmaceuticals Inc.
  • 66220-815 Reditrex 15 mg/.6ml Subcutaneous Injection, Solution by Cumberland Pharmaceuticals Inc.
  • 66220-817 Reditrex 17.5 mg/.7ml Subcutaneous Injection, Solution by Cumberland Pharmaceuticals Inc.
  • 66220-820 Reditrex 20 mg/.8ml Subcutaneous Injection, Solution by Cumberland Pharmaceuticals Inc.
  • 66220-822 Reditrex 22.5 mg/.9ml Subcutaneous Injection, Solution by Cumberland Pharmaceuticals Inc.
  • 66220-825 Reditrex 25 mg/ml Subcutaneous Injection, Solution by Cumberland Pharmaceuticals 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.