54569-5785 : Cefprozil 250 mg/5ml Oral Powder, for Suspension


NDC: 54569-5785
Labeler: A-s Medication Solutions LLC
Product Type: Human Prescription Drug
Drug Name:  Cefprozil
Dosage Form: Oral Powder, for Suspension
Application #: ANDA065261
Rev. Date: 


NDC Package Codes:

  • 54569-5785-0: 100 ML IN 1 BOTTLE (54569‑5785‑0)

Active Ingredients:

  • Cefprozil

Dosage Strength:

  • 250 mg/5mL

Related Products:

Based on records with the same trade name.
  • 54569-5784 Cefprozil 250 mg Oral Tablet by A-s Medication Solutions LLC
  • 54569-6195 Cefprozil 500 mg Oral Tablet by A-s Medication Solutions LLC
  • 0093-1075 Cefprozil 125 mg/5ml Oral Powder, for Suspension by Teva Pharmaceuticals USA Inc
  • 0093-1076 Cefprozil 250 mg/5ml Oral Powder, for Suspension by Teva Pharmaceuticals USA Inc
  • 0093-1077 Cefprozil 250 mg Oral Tablet by Teva Pharmaceuticals USA Inc
  • 0093-1078 Cefprozil 500 mg Oral Tablet by Teva Pharmaceuticals USA Inc
  • 0781-5043 Cefprozil 250 mg Oral Tablet by Sandoz Inc
  • 0781-5044 Cefprozil 500 mg Oral Tablet by Sandoz Inc
  • 0781-6202 Cefprozil 125 mg/5ml Oral Powder, for Suspension by Sandoz Inc
  • 0781-6203 Cefprozil 250 mg/5ml Oral Powder, for Suspension by Sandoz Inc
  • 16714-208 Cefprozil 250 mg Oral Tablet by Northstar Rx LLC
  • 16714-209 Cefprozil 500 mg Oral Tablet by Northstar Rx LLC
  • 16714-386 Cefprozil 125 mg/5ml Oral Powder, for Suspension by Northstar Rx LLC
  • 16714-387 Cefprozil 250 mg/5ml Oral Powder, for Suspension by Northstar Rx LLC
  • 16714-396 Cefprozil 125 mg/5ml Oral Powder, for Suspension by Northstar Rx LLC
  • 16714-397 Cefprozil 250 mg/5ml Oral Powder, for Suspension by Northstar Rx LLC
  • 16714-398 Cefprozil 250 mg Oral Tablet by Northstar Rx LLC
  • 16714-399 Cefprozil 500 mg Oral Tablet by Northstar Rx LLC
  • 42043-262 Cefprozil 125 mg/5ml Oral Powder, for Suspension by Orchidpharma Inc
  • 42043-263 Cefprozil 250 mg/5ml Oral Powder, for Suspension by Orchidpharma Inc
  • More related products ...

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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.