NDC 0085-1341

ASMANEX

Mometasone Furoate

ASMANEX is a Respiratory (inhalation) Inhalant in the Human Prescription Drug category. It is labeled and distributed by Merck Sharp & Dohme Corp.. The primary component is Mometasone Furoate.

Product ID0085-1341_22ce7e61-648f-4680-b024-f35096bf5d82
NDC0085-1341
Product TypeHuman Prescription Drug
Proprietary NameASMANEX
Generic NameMometasone Furoate
Dosage FormInhalant
Route of AdministrationRESPIRATORY (INHALATION)
Marketing Start Date2005-03-30
Marketing CategoryNDA / NDA
Application NumberNDA021067
Labeler NameMerck Sharp & Dohme Corp.
Substance NameMOMETASONE FUROATE
Active Ingredient Strength220 ug/1
Pharm ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid Hormone Receptor Agonists [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0085-1341-01

1 POUCH in 1 CARTON (0085-1341-01) > 1 INHALER in 1 POUCH > 120 INHALANT in 1 INHALER
Marketing Start Date2005-03-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0085-1341-06 [00085134106]

ASMANEX INHALANT
Marketing CategoryNDA
Application NumberNDA021067
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-03-30

NDC 0085-1341-01 [00085134101]

ASMANEX INHALANT
Marketing CategoryNDA
Application NumberNDA021067
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-03-30

NDC 0085-1341-05 [00085134105]

ASMANEX INHALANT
Marketing CategoryNDA
Application NumberNDA021067
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2005-03-30

NDC 0085-1341-03 [00085134103]

ASMANEX INHALANT
Marketing CategoryNDA
Application NumberNDA021067
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-03-30
Marketing End Date2014-10-07

NDC 0085-1341-04 [00085134104]

ASMANEX INHALANT
Marketing CategoryNDA
Application NumberNDA021067
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-03-30
Marketing End Date2015-01-31

NDC 0085-1341-02 [00085134102]

ASMANEX INHALANT
Marketing CategoryNDA
Application NumberNDA021067
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-03-30

NDC 0085-1341-07 [00085134107]

ASMANEX INHALANT
Marketing CategoryNDA
Application NumberNDA021067
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-03-30

Drug Details

Active Ingredients

IngredientStrength
MOMETASONE FUROATE220 ug/1

OpenFDA Data

SPL SET ID:1ec2b62b-6bf5-4d70-8824-9d90e2d87a68
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 746812
  • 746813
  • 746803
  • 746811
  • 746804
  • 746814
  • 746815
  • 790280
  • 790283
  • 790284
  • 790278
  • 746810

    • Pharmacological Class

    • Corticosteroid [EPC]
    • Corticosteroid Hormone Receptor Agonists [MoA]
    • Corticosteroid Hormone Receptor Agonists [MoA]

    NDC Crossover Matching brand name "ASMANEX" or generic name "Mometasone Furoate"

    NDCBrand NameGeneric Name
    0085-1341ASMANEXMometasone Furoate
    0085-1461ASMANEXMometasone Furoate
    0085-2222ASMANEX HFAMOMETASONE FUROATE
    0085-4333ASMANEX HFAMOMETASONE FUROATE
    0085-4334ASMANEX HFAMOMETASONE FUROATE
    0085-0370ELOCONmometasone furoate
    0085-0854ELOCONMometasone Furoate
    0085-3149ELOCONMometasone Furoate
    0168-0270Mometasone Furoatemometasone furoate
    0168-0271Mometasone Furoatemometasone furoate
    0168-0272Mometasone Furoatemometasone furoate
    0713-0634Mometasone FuroateMometasone Furoate
    0113-1720Nasonexmometasone furoate

    Trademark Results [ASMANEX]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    ASMANEX
    ASMANEX
    78489101 3127884 Dead/Cancelled
    MERCK SHARP & DOHME CORP.
    2004-09-24
    ASMANEX
    ASMANEX
    76029251 not registered Dead/Abandoned
    SCHERING CORPORATION
    2000-04-18
    ASMANEX
    ASMANEX
    74462173 2136067 Live/Registered
    MERCK SHARP & DOHME CORP.
    1993-11-22
    © 2025 FDA.report
    This site is not affiliated with or endorsed by the FDA.