52652-8001 : Zonisade 100 mg/5ml Oral Suspension


NDC52652-8001
Labeler: Azurity Phramaceuticals, Inc.
Product Type: Human Prescription Drug
Drug Name:  Zonisade
Dosage Form: Oral Suspension
Application #: NDA214273
Rev. Date: 


NDC Package Codes:

  • 52652-8001-1: 1 BOTTLE IN 1 CARTON (52652‑8001‑1) > 150 ML IN 1 BOTTLE

Active Ingredients:

  • Zonisamide

Dosage Strength:

  • 100 mg/5mL

Pharmaceutical Classes:

  • Anti-epileptic Agent [EPC]
  • Carbonic Anhydrase Inhibitors [MoA]
  • Decreased Central Nervous System Disorganized Electrical Activity [PE]
  • P-Glycoprotein Inhibitors [MoA]
  • Sulfonamides [CS]

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