propecia

Generic: finasteride

Labeler: organon llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name propecia
Generic Name finasteride
Labeler organon llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

finasteride 1 mg/1

Manufacturer
Organon LLC

Identifiers & Regulatory

Product NDC 78206-152
Product ID 78206-152_97f5deb0-a4ab-42c3-afa0-db2170a16297
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020788
Listing Expiration 2026-12-31
Marketing Start 2021-06-01

Pharmacologic Class

Established (EPC)
5-alpha reductase inhibitor [epc]
Mechanism of Action
5-alpha reductase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 78206152
Hyphenated Format 78206-152

Supplemental Identifiers

RxCUI
200172 213178
UPC
0378206152015
UNII
57GNO57U7G
NUI
N0000175836 N0000000126

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name propecia (source: ndc)
Generic Name finasteride (source: ndc)
Application Number NDA020788 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (78206-152-01)
  • 90 TABLET, FILM COATED in 1 BOTTLE (78206-152-02)
source: ndc

Packages (2)

78206-152-01 30 TABLET, FILM COATED in 1 BOTTLE (78206-152-01) 78206-152-02 90 TABLET, FILM COATED in 1 BOTTLE (78206-152-02)

Ingredients (1)

finasteride (1 mg/1)

Linked Drug Pages (1)

PROPECIA ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "97f5deb0-a4ab-42c3-afa0-db2170a16297", "openfda": {"nui": ["N0000175836", "N0000000126"], "upc": ["0378206152015"], "unii": ["57GNO57U7G"], "rxcui": ["200172", "213178"], "spl_set_id": ["6f904709-65aa-44ce-b144-b4c8a0416e36"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Organon LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (78206-152-01)", "package_ndc": "78206-152-01", "marketing_start_date": "20210601"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (78206-152-02)", "package_ndc": "78206-152-02", "marketing_start_date": "20210601"}], "brand_name": "PROPECIA", "product_id": "78206-152_97f5deb0-a4ab-42c3-afa0-db2170a16297", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "78206-152", "generic_name": "finasteride", "labeler_name": "Organon LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROPECIA", "active_ingredients": [{"name": "FINASTERIDE", "strength": "1 mg/1"}], "application_number": "NDA020788", "marketing_category": "NDA", "marketing_start_date": "20210601", "listing_expiration_date": "20261231"}