0088-1208 : Anzemet 12.5 mg/.625ml Intravenous Injection


NDC: 0088-1208
Labeler: Sanofi-aventis U.S. LLC
Product Type: Human Prescription Drug
Drug Name:  Anzemet
Dosage Form: Intravenous Injection
Application #: NDA020624
Rev. Date: 


NDC Package Codes:

  • 0088-1208-06: 6 VIAL, SINGLE‑USE IN 1 BOX (0088‑1208‑06) > .625 ML IN 1 VIAL, SINGLE‑USE

Active Ingredients:

  • Dolasetron Mesylate

Dosage Strength:

  • 12.5 mg/.625mL

Pharmaceutical Classes:

  • Serotonin 3 Receptor Antagonists [MoA]
  • Serotonin-3 Receptor Antagonist [EPC]

Related Products:

Based on records with the same trade name.
  • 0088-1202 Anzemet 50 mg Oral Tablet by Sanofi-aventis U.S. LLC
  • 0088-1203 Anzemet 100 mg Oral Tablet by Sanofi-aventis U.S. LLC
  • 0088-1206 Anzemet 100 mg/5ml Intravenous Injection by Sanofi-aventis U.S. LLC
  • 0088-1209 Anzemet 500 mg/25ml Intravenous Injection by Sanofi-aventis U.S. LLC
  • 30698-120 Anzemet 50 mg Oral Tablet, Film Coated by Validus Pharmaceuticals LLC
  • 30698-121 Anzemet 100 mg Oral Tablet, Film Coated by Validus Pharmaceuticals LLC
  • 30698-220 Anzemet 50 mg Oral Tablet, Film Coated by Validus Pharmaceuticals LLC
  • 69189-0679 Anzemet 100 mg Oral Tablet, Film Coated by Avera Mckennan Hospital

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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.