FDA.reportPublic FDA data

FLOVENT

Product NDC
0173-0600
11-digit product format
001730600
Labeler code
0173
Product ID
0173-0600_995f7d42-c1ba-4de2-aff5-9b02187ab606
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
fluticasone propionate
Dosage form
POWDER, METERED
Route
RESPIRATORY (INHALATION)
Labeler
GlaxoSmithKline LLC
Application
NDA020833
Marketing category
NDA
Marketing start
2007-05-08
Marketing end
0000-00-00
Substance
FLUTICASONE PROPIONATE
Active strength
50 ug/1
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f4fb2f5a-dadb-40e3-a4b1-a2a58f5d9a33Product name320260126
343e8617-eb68-1e10-cfa9-8c30af285764Product name320240513
a31ad3df-8021-2ea1-94eb-0fe2f49b7729Product name420220719
813fe018-3e3c-40e4-8f71-7ab50f3dfe81Product name220180723
3bcd721e-0555-4bc3-96c6-690471ff9d94Product name120171113
9f9452df-fa34-43d4-97fe-c6605344c5a8Product name120171113
0e5a25a6-9f05-44b5-8449-aa63e59f7202Product name120170426
f3c5232f-03de-44f5-996a-90cd9c08bc60Product name120170426
1cb17fbb-0da4-2841-37bc-e7079783e1a2Product name120140508
667f427a-8698-a508-767a-53ed61b4c2e9Product name120140508
6a97ffc8-1d4d-a971-4978-85ba3a22eac9Product name120140508
6df84e13-2223-fa46-1e26-17e2f58a1e1cProduct name120140508
90fec588-984c-4375-cfd4-7e40114bdf80Product name120140508
9c1d3c48-b162-204b-f55b-e0f25c31c52eProduct name120140508
9fdb6139-394b-1510-4baf-bde68c419789Product name120140508
aef26912-037b-9a4e-db49-225ef6dfd8f1Product name120140508

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0173-0600-02EA - Each0173-0600d113dcba-b009-44bd-a2fc-d02d593c2b6512012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FLUTICASONE PROPIONATEACTIVE INGREDIENTO2GMZ0LF5WFLOVENT DISKUS (FLUTICASONE PROPIONATE) POWDER, METERED [GLAXOSMITHKLINE LLC]19
FLUTICASONEACTIVE MOIETYCUT2W21N7UFLOVENT DISKUS (FLUTICASONE PROPIONATE) POWDER, METERED [GLAXOSMITHKLINE LLC]19
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GFLOVENT DISKUS (FLUTICASONE PROPIONATE) POWDER, METERED [GLAXOSMITHKLINE LLC]19

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0173-0600FLOVENT DISKUS (FLUTICASONE PROPIONATE) POWDER, METERED [GLAXOSMITHKLINE LLC]34Legacy NDC20240915_001f22f8-a83d-495f-9196-d0264ef4d76e.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
896019Flovent Diskus 50 MCG/INHAL Dry Powder Inhaler, 60 BlistersPSN038e6c40-9421-40ef-874b-8f4d7110a74a14
896018fluticasone propionate 50 MCG/INHAL Dry Powder Inhaler, 60 BlistersPSN038e6c40-9421-40ef-874b-8f4d7110a74a14
89601960 ACTUAT fluticasone propionate 0.05 MG/ACTUAT Dry Powder Inhaler [Flovent]SBD038e6c40-9421-40ef-874b-8f4d7110a74a14
89601860 ACTUAT fluticasone propionate 0.05 MG/ACTUAT Dry Powder InhalerSCD038e6c40-9421-40ef-874b-8f4d7110a74a14
89601960 ACTUAT Flovent 0.05 MG/ACTUAT Dry Powder InhalerSY038e6c40-9421-40ef-874b-8f4d7110a74a14
896019Flovent Diskus 0.05 MG/ACTUAT Dry Powder Inhaler, 60 ACTUATSY038e6c40-9421-40ef-874b-8f4d7110a74a14
896019Flovent Diskus 50 MCG/ACTUAT Dry Powder Inhaler, 60 ACTUATSY038e6c40-9421-40ef-874b-8f4d7110a74a14
896018fluticasone propionate 0.05 MG/ACTUAT Dry Powder Inhaler, 60 ACTUATSY038e6c40-9421-40ef-874b-8f4d7110a74a14

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0173-0600-02001730600021 INHALER in 1 CARTON (0173-0600-02) > 60 POWDER, METERED in 1 INHALER1 inhaler2007-05-080000-00-00NoNoCurrent