SYMBICORT - 0186-0370-20 - (Budesonide and Formoterol Fumarate Dihydrate)

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Drug Information of SYMBICORT

Product NDC: 0186-0370
Proprietary Name: SYMBICORT
Non Proprietary Name: Budesonide and Formoterol Fumarate Dihydrate
Active Ingredient(s): 160; 4.5    ug/1; ug/1 & nbsp;   Budesonide and Formoterol Fumarate Dihydrate
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): AEROSOL
Coding System: National Drug Codes(NDC)

Labeler Information of SYMBICORT

Product NDC: 0186-0370
Labeler Name: AstraZeneca LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021929
Marketing Category: NDA
Start Marketing Date: 20070529

Package Information of SYMBICORT

Package NDC: 0186-0370-20
Package Description: 1 POUCH in 1 CARTON (0186-0370-20) > 1 CANISTER in 1 POUCH > 120 AEROSOL in 1 CANISTER

NDC Information of SYMBICORT

NDC Code 0186-0370-20
Proprietary Name SYMBICORT
Package Description 1 POUCH in 1 CARTON (0186-0370-20) > 1 CANISTER in 1 POUCH > 120 AEROSOL in 1 CANISTER
Product NDC 0186-0370
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Budesonide and Formoterol Fumarate Dihydrate
Dosage Form Name AEROSOL
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20070529
Marketing Category Name NDA
Labeler Name AstraZeneca LP
Substance Name BUDESONIDE; FORMOTEROL FUMARATE DIHYDRATE
Strength Number 160; 4.5
Strength Unit ug/1; ug/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of SYMBICORT


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