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PULMICORT RESPULES - 55154-9613-5 - (Budesonide)

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Drug Information of PULMICORT RESPULES

Product NDC: 55154-9613
Proprietary Name: PULMICORT RESPULES
Non Proprietary Name: Budesonide
Active Ingredient(s): .5    mg/2mL & nbsp;   Budesonide
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of PULMICORT RESPULES

Product NDC: 55154-9613
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020929
Marketing Category: NDA
Start Marketing Date: 20091120

Package Information of PULMICORT RESPULES

Package NDC: 55154-9613-5
Package Description: 5 AMPULE in 1 BAG (55154-9613-5) > 2 mL in 1 AMPULE

NDC Information of PULMICORT RESPULES

NDC Code 55154-9613-5
Proprietary Name PULMICORT RESPULES
Package Description 5 AMPULE in 1 BAG (55154-9613-5) > 2 mL in 1 AMPULE
Product NDC 55154-9613
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Budesonide
Dosage Form Name SUSPENSION
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20091120
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name BUDESONIDE
Strength Number .5
Strength Unit mg/2mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of PULMICORT RESPULES


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