0310-7372 : Budesonide and Formoterol Fumarate Dihydrate Respiratory (Inhalation) Aerosol


NDC: 0310-7372
Labeler: Astrazeneca Pharmaceuticals Lp
Product Type: Human Prescription Drug
Drug Name:  Budesonide and Formoterol Fumarate Dihydrate
Dosage Form: Respiratory (Inhalation) Aerosol
Application #: NDA021929
Rev. Date: 


NDC Package Codes:

  • 0310-7372-20: 1 POUCH IN 1 CARTON (0310‑7372‑20) > 1 CANISTER IN 1 POUCH > 120 AEROSOL IN 1 CANISTER

Active Ingredients:

  • Budesonide
  • Formoterol Fumarate

Dosage Strength:

  • 80 ug/1
  • 4.5 ug/1

Pharmaceutical Classes:

  • Corticosteroid [EPC]
  • Corticosteroid Hormone Receptor Agonists [MoA]
  • Adrenergic beta2-Agonists [MoA]
  • beta2-Adrenergic Agonist [EPC]

Related Products:

Based on records with the same trade name.
  • 0310-7370 Budesonide and Formoterol Fumarate Dihydrate Respiratory (Inhalation) Aerosol by Astrazeneca Pharmaceuticals Lp
  • 50090-6327 Budesonide and Formoterol Fumarate Dihydrate Respiratory (Inhalation) Aerosol by A-s Medication Solutions
  • 50090-6382 Budesonide and Formoterol Fumarate Dihydrate Respiratory (Inhalation) Aerosol by A-s Medication Solutions
  • 53002-2666 Budesonide and Formoterol Fumarate Dihydrate Respiratory (Inhalation) Aerosol by Rpk Pharmaceuticals, Inc.
  • 53002-2667 Budesonide and Formoterol Fumarate Dihydrate Respiratory (Inhalation) Aerosol by Rpk Pharmaceuticals, Inc.
  • 70518-3107 Budesonide and Formoterol Fumarate Dihydrate Respiratory (Inhalation) Aerosol by Remedyrepack 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.