Finasteride

Product NDC
0904-6830
11-digit product format
009046830
Labeler code
0904
Product ID
0904-6830_d1f34c55-de1d-48a5-af38-06cbea8c6b8d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Finasteride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Major Pharmaceuticals
Application
ANDA090061
Marketing category
ANDA
Marketing start
2015-06-13
Substance
FINASTERIDE
Active strength
5 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
Finasteride
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
FINASTERIDE5 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii57GNO57U7G
Rxcui310346

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
0904-6830-06Finasteride50 in 1 CARTONTABLET, FILM COATED507
0904-6830-06Finasteride1 in 1 BLISTER PACKTABLET, FILM COATED17
0904-6830-61Finasteride100 in 1 CARTONTABLET, FILM COATED1007
0904-6830-61Finasteride1 in 1 BLISTER PACKTABLET, FILM COATED17

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0904-6830-06EA - Each0904-683015d405f2-11a2-4b32-8ddb-a941e2b501db12019-04-11
0904-6830-61EA - Each0904-6830534519d6-7bbd-4f9b-a6de-65c51372a50212019-04-11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0904-6830FINASTERIDE TABLET, FILM COATED [MAJOR PHARMACEUTICALS]6Current NDC, Legacy NDC, 4 package rows20250207_3272651f-b500-4d5d-9e29-22fcd8e24fcb.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310346finasteride 5 MG Oral TabletPSN3fec2bcb-91b8-4041-9ee8-e5a4ebe5fd048
310346finasteride 5 MG Oral TabletSCD3fec2bcb-91b8-4041-9ee8-e5a4ebe5fd048
310346FIN5C 5 MG Oral TabletSY3fec2bcb-91b8-4041-9ee8-e5a4ebe5fd048
310346finasteride 5 MG Oral TabletPSN3272651f-b500-4d5d-9e29-22fcd8e24fcb7
310346finasteride 5 MG Oral TabletSCD3272651f-b500-4d5d-9e29-22fcd8e24fcb7
310346FIN5C 5 MG Oral TabletSY3272651f-b500-4d5d-9e29-22fcd8e24fcb7
310346finasteride 5 MG Oral TabletPSN22161236-6804-4a7f-86cb-cfa20bd1951e3
310346finasteride 5 MG Oral TabletSCD22161236-6804-4a7f-86cb-cfa20bd1951e3
310346FIN5C 5 MG Oral TabletSY22161236-6804-4a7f-86cb-cfa20bd1951e3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0904-6830-060090468300650 BLISTER PACK in 1 CARTON (0904-6830-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK50 blister pack2015-06-130000-00-00NoNoCurrent
0904-6830-6100904683061100 BLISTER PACK in 1 CARTON (0904-6830-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK100 blister pack2015-06-130000-00-00NoNoCurrent