ASMANEX HFA

Product NDC
0085-2222
11-digit product format
000852222
Labeler code
0085
Product ID
0085-2222_44a6c4f5-761f-4192-a10e-faf566e7864f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
MOMETASONE FUROATE
Dosage form
AEROSOL
Route
RESPIRATORY (INHALATION)
Labeler
Merck Sharp & Dohme Corp.
Application
NDA205641
Marketing category
NDA
Marketing start
2019-08-12
Marketing end
0000-00-00
Substance
MOMETASONE FUROATE
Active strength
50 ug/1
Pharmacologic classes
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0085-2222-01GM - Gram0085-2222edbcfae5-5eb4-4b35-844d-b439bafb819f12020-02-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0085-2222-01000852222011 CANISTER in 1 CARTON (0085-2222-01) > 120 AEROSOL in 1 CANISTER1 canister2019-08-120000-00-00NoNoCurrent
0085-2222-02000852222021 CANISTER in 1 CARTON (0085-2222-02) > 120 AEROSOL in 1 CANISTER1 canister2019-08-120000-00-00NoNoCurrent