51672-1338 : Flo-pred 15 mg/5ml Oral Suspension


NDC: 51672-1338
Labeler: Taro Pharmaceuticals U.S.a., Inc.
Product Type: Human Prescription Drug
Drug Name:  Flo-pred
Dosage Form: Oral Suspension
Application #: NDA022067
Rev. Date: 


NDC Package Codes:

  • 51672-1338-3: 1 BOTTLE IN 1 CARTON (51672‑1338‑3) > 52 ML IN 1 BOTTLE
  • 51672-1338-5: 1 BOTTLE IN 1 CARTON (51672‑1338‑5) > 37 ML IN 1 BOTTLE
  • 51672-1338-6: 1 BOTTLE IN 1 CARTON (51672‑1338‑6) > 65 ML IN 1 BOTTLE

Active Ingredients:

  • Prednisolone Acetate

Dosage Strength:

  • 16.7 mg/5mL

Pharmaceutical Classes:

  • Corticosteroid Hormone Receptor Agonists [MoA]
  • Corticosteroid [EPC]

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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.