54436-020 : Otrexup 20 mg/.4ml Subcutaneous Injection, Solution


NDC54436-020
Labeler: Antares Pharma, Inc.
Product Type: Human Prescription Drug
Drug Name:  Otrexup
Dosage Form: Subcutaneous Injection, Solution
Application #: NDA204824
Rev. Date: 


NDC Package Codes:

  • 54436-020-01: 1 SYRINGE IN 1 CARTON (54436‑020‑01) > .4 ML IN 1 SYRINGE
  • 54436-020-03: 1 SYRINGE IN 1 CARTON (54436‑020‑03) > .4 ML IN 1 SYRINGE
  • 54436-020-04: 4 SYRINGE IN 1 CARTON (54436‑020‑04) > .4 ML IN 1 SYRINGE (54436‑020‑02)

Active Ingredients:

  • Methotrexate

Dosage Strength:

  • 20 mg/.4mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 54436-010 Otrexup 10 mg/.4ml Subcutaneous Injection, Solution by Antares Pharma, Inc.
  • 54436-012 Otrexup 12.5 mg/.4ml Subcutaneous Injection, Solution by Antares Pharma, Inc.
  • 54436-015 Otrexup 15 mg/.4ml Subcutaneous Injection, Solution by Antares Pharma, Inc.
  • 54436-017 Otrexup 17.5 mg/.4ml Subcutaneous Injection, Solution by Antares Pharma, Inc.
  • 54436-022 Otrexup 22.5 mg/.4ml Subcutaneous Injection, Solution by Antares Pharma, Inc.
  • 54436-025 Otrexup 25 mg/.4ml Subcutaneous Injection, Solution by Antares Pharma, Inc.
  • 54436-075 Otrexup 7.5 mg/.4ml Subcutaneous Injection, Solution by Antares Pharma, 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.