55150-174 : Azithromycin 500 mg Intravenous Injection, Powder, Lyophilized, for Solution


NDC: 55150-174
Labeler: Auromedics Pharma LLC
Product Type: Human Prescription Drug
Drug Name:  Azithromycin
Dosage Form: Intravenous Injection, Powder, Lyophilized, for Solution
Application #: ANDA203294
Rev. Date: 


NDC Package Codes:

  • 55150-174-10: 10 VIAL IN 1 CARTON (55150‑174‑10) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION IN 1 VIAL

Active Ingredients:

  • Azithromycin Monohydrate

Dosage Strength:

  • 500 mg

Pharmaceutical Classes:

  • Macrolide Antimicrobial [EPC]
  • Macrolides [CS]

Related Products:

Based on records with the same trade name.
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  • 0093-7147 Azithromycin 600 mg Oral Tablet by Teva Pharmaceuticals USA Inc
  • 0093-7148 Azithromycin 100 mg/5ml Oral Powder, for Suspension by Teva Pharmaceuticals USA Inc
  • 0093-7149 Azithromycin 200 mg/5ml Oral Powder, for Suspension by Teva Pharmaceuticals USA Inc
  • 0093-7169 Azithromycin 500 mg Oral Tablet 3 Count Pack by Teva Pharmaceuticals USA Inc
  • 0179-0033 Azithromycin 600 mg Oral Tablet by Kaiser Foundation Hospitals
  • 0409-0144 Azithromycin 500 mg/1 Intravenous Injection, Powder, Lyophilized, for Solution by Hospira, Inc.
  • 0527-2370 Azithromycin 250 mg Oral Tablet, Film Coated by Lannett Company, Inc.
  • 0527-2381 Azithromycin 600 mg Oral Tablet, Film Coated by Lannett Company, Inc.
  • 0527-2395 Azithromycin 500 mg Oral Tablet, Film Coated by Lannett Company, Inc.
  • 0781-1496 Azithromycin 250 mg Oral Tablet 6 Count Pack by Sandoz Inc
  • 0781-1497 Azithromycin 600 mg Oral Tablet by Sandoz Inc
  • 0781-1941 Azithromycin 500 mg Oral Tablet 3 Count Pack by Sandoz Inc
  • 0781-5776 Azithromycin 250 mg Oral Tablet, Film Coated by Sandoz Inc
  • 0781-5789 Azithromycin 500 mg Oral Tablet, Film Coated by Sandoz Inc
  • 0781-5793 Azithromycin 600 mg Oral Tablet, Film Coated by Sandoz Inc
  • 0781-8089 Azithromycin 250 mg Oral Tablet, Film Coated by Sandoz Inc
  • 0781-8090 Azithromycin 500 mg Oral Tablet, Film Coated by Sandoz 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.