Dulera - 0085-7206-02 - (mometasone furoate and formoterol fumarate dihydrate)

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Drug Information of Dulera

Product NDC: 0085-7206
Proprietary Name: Dulera
Non Proprietary Name: mometasone furoate and formoterol fumarate dihydrate
Active Ingredient(s): 5; 100    ug/1; ug/1 & nbsp;   mometasone furoate and formoterol fumarate dihydrate
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): AEROSOL
Coding System: National Drug Codes(NDC)

Labeler Information of Dulera

Product NDC: 0085-7206
Labeler Name: Merck Sharp & Dohme Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022518
Marketing Category: NDA
Start Marketing Date: 20100622

Package Information of Dulera

Package NDC: 0085-7206-02
Package Description: 1 CANISTER in 1 CARTON (0085-7206-02) > 120 AEROSOL in 1 CANISTER

NDC Information of Dulera

NDC Code 0085-7206-02
Proprietary Name Dulera
Package Description 1 CANISTER in 1 CARTON (0085-7206-02) > 120 AEROSOL in 1 CANISTER
Product NDC 0085-7206
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name mometasone furoate and formoterol fumarate dihydrate
Dosage Form Name AEROSOL
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20100622
Marketing Category Name NDA
Labeler Name Merck Sharp & Dohme Corp.
Substance Name FORMOTEROL FUMARATE DIHYDRATE; MOMETASONE FUROATE
Strength Number 5; 100
Strength Unit ug/1; ug/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid Hormone Receptor Agonists [MoA],Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of Dulera


General Information