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PULMICORT RESPULES - 54868-5774-0 - (Budesonide)

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Drug Information of PULMICORT RESPULES

Product NDC: 54868-5774
Proprietary Name: PULMICORT RESPULES
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 PULMICORT RESPULES

Product NDC: 54868-5774
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020929
Marketing Category: NDA
Start Marketing Date: 20070601

Package Information of PULMICORT RESPULES

Package NDC: 54868-5774-0
Package Description: 6 POUCH in 1 CARTON (54868-5774-0) > 5 AMPULE in 1 POUCH > 2 mL in 1 AMPULE

NDC Information of PULMICORT RESPULES

NDC Code 54868-5774-0
Proprietary Name PULMICORT RESPULES
Package Description 6 POUCH in 1 CARTON (54868-5774-0) > 5 AMPULE in 1 POUCH > 2 mL in 1 AMPULE
Product NDC 54868-5774
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Budesonide
Dosage Form Name SUSPENSION
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20070601
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name BUDESONIDE
Strength Number .25
Strength Unit mg/2mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of PULMICORT RESPULES


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