NDC 0093-6816 – Budesonide

Budesonide .5 mg/2mL · Suspension · Respiratory (inhalation)

Human Prescription Drug

Product NDC0093-6816

Product details

Brand name
Budesonide
Generic name
Budesonide
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Suspension
Route
Respiratory (inhalation)
Marketing category
ANDA · ANDA077519
Marketed since
November 19, 2008
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Budesonide →

Package NDC codes (3)

Package NDCDescriptionSince
0093-6816-5530 POUCH in 1 CARTON (0093-6816-55) / 1 VIAL, SINGLE-DOSE in 1 POUCH / 2 mL in 1 VIAL, SINGLE-DOSEJan 11, 2019
0093-6816-736 POUCH in 1 CARTON (0093-6816-73) / 5 VIAL, SINGLE-DOSE in 1 POUCH (0093-6816-45) / 2 mL in 1 VIAL, SINGLE-DOSE (0093-6816-19)Nov 19, 2008
0093-6816-762 POUCH in 1 CARTON (0093-6816-76) / 5 VIAL, SINGLE-DOSE in 1 POUCH / 2 mL in 1 VIAL, SINGLE-DOSENov 19, 2008

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