Budesonide - 0093-6815-76 - (Budesonide)

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Drug Information of Budesonide

Product NDC: 0093-6815
Proprietary Name: Budesonide
Non Proprietary Name: Budesonide
Active Ingredient(s): .25    mg/2mL & nbsp;   Budesonide
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Budesonide

Product NDC: 0093-6815
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077519
Marketing Category: ANDA
Start Marketing Date: 20081119

Package Information of Budesonide

Package NDC: 0093-6815-76
Package Description: 2 POUCH in 1 CARTON (0093-6815-76) > 5 VIAL, SINGLE-DOSE in 1 POUCH > 2 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Budesonide

NDC Code 0093-6815-76
Proprietary Name Budesonide
Package Description 2 POUCH in 1 CARTON (0093-6815-76) > 5 VIAL, SINGLE-DOSE in 1 POUCH > 2 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0093-6815
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Budesonide
Dosage Form Name SUSPENSION
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20081119
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name BUDESONIDE
Strength Number .25
Strength Unit mg/2mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Budesonide


General Information