NDC 0310-7372 – Budesonide and Formoterol Fumarate Dihydrate

Budesonide 80 ug/1; Formoterol Fumarate 4.5 ug/1 · Aerosol · Respiratory (inhalation)

Human Prescription Drug 1 recall

Product NDC0310-7372

Product details

Brand name
Budesonide and Formoterol Fumarate Dihydrate
Generic name
Budesonide and Formoterol Fumarate Dihydrate
Labeler
AstraZeneca Pharmaceuticals LP
Dosage form
Aerosol
Route
Respiratory (inhalation)
Marketing category
NDA AUTHORIZED GENERIC · NDA021929
Marketed since
January 3, 2020
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid; beta2-Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Budesonide and Formoterol Fumarate Dihydrate →

Package NDC codes (1)

Package NDCDescriptionSince
0310-7372-201 POUCH in 1 CARTON (0310-7372-20) / 1 CANISTER in 1 POUCH / 120 AEROSOL in 1 CANISTERJan 3, 2020

Recalls mentioning this NDC

Other Budesonide and Formoterol Fumarate Dihydrate products