PROPECIA

Product NDC
78206-152
11-digit product format
782060152
Labeler code
78206
Product ID
78206-152_97f5deb0-a4ab-42c3-afa0-db2170a16297
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
finasteride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Organon LLC
Application
NDA020788
Marketing category
NDA
Marketing start
2021-06-01
Substance
FINASTERIDE
Active strength
1 mg/1
Pharmacologic classes
5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
PROPECIA
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
FINASTERIDE1 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii57GNO57U7G
Rxcui200172, 213178

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
928d249c-35c3-4d88-a9ef-cf2f2e31b96fProduct name120220706
d00474ae-23eb-a8eb-bf56-520e590cc6dbProduct name220170406
0f90664c-9d0e-f046-dc6a-73563cd8347eProduct name220170405

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78206-152-01PROPECIA30 in 1 BOTTLETABLET, FILM COATED309
78206-152-02PROPECIA90 in 1 BOTTLETABLET, FILM COATED909

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
78206-152-01EA - Each78206-1525942a252-dd75-42cf-a43c-f9f6363fb07612021-08-05
78206-152-02EA - Each78206-152b7a02e47-9d01-42e4-b574-62b65864accc12021-08-05

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78206-152PROPECIA (FINASTERIDE) TABLET, FILM COATED [ORGANON LLC]9Current NDC, Legacy NDC, 2 package rows20241013_6f904709-65aa-44ce-b144-b4c8a0416e36.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
200172finasteride 1 MG Oral TabletPSN6f904709-65aa-44ce-b144-b4c8a0416e369
213178Propecia 1 MG Oral TabletPSN6f904709-65aa-44ce-b144-b4c8a0416e369
213178finasteride 1 MG Oral Tablet [Propecia]SBD6f904709-65aa-44ce-b144-b4c8a0416e369
200172finasteride 1 MG Oral TabletSCD6f904709-65aa-44ce-b144-b4c8a0416e369
200172FIN5C 1 MG Oral TabletSY6f904709-65aa-44ce-b144-b4c8a0416e369
213178FIN5C 1 MG Oral Tablet [Propecia]SY6f904709-65aa-44ce-b144-b4c8a0416e369
213178Propecia 1 MG Oral TabletSY6f904709-65aa-44ce-b144-b4c8a0416e369

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
78206-152-017820601520130 TABLET, FILM COATED in 1 BOTTLE (78206-152-01) 2021-06-010000-00-00NoNoCurrent
78206-152-027820601520290 TABLET, FILM COATED in 1 BOTTLE (78206-152-02) 2021-06-010000-00-00NoNoCurrent