59368-403 : Myhibbin 200 mg/ml Oral Suspension


NDC: 59368-403
Labeler: Praxis, LLC
Product Type: Human Prescription Drug
Drug Name:  Myhibbin
Dosage Form: Oral Suspension
Application #: NDA216482
Rev. Date: 


NDC Package Codes:

  • 59368-403-01: 1 BOTTLE, PLASTIC IN 1 CARTON (59368‑403‑01) / 175 ML IN 1 BOTTLE, PLASTIC

Active Ingredients:

  • Mycophenolate Mofetil

Dosage Strength:

  • 200 mg/mL

Pharmaceutical Classes:

  • Antimetabolite Immunosuppressant [EPC]

Related Products:

Based on records with the same trade name.
  • 24338-018 Myhibbin 200 mg/ml Oral Suspension by Azurity 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.