dutasteride

Generic: dutasteride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dutasteride
Generic Name dutasteride
Labeler proficient rx lp
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

dutasteride .5 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-039
Product ID 71205-039_4ca84780-9497-4cc3-a5bb-01b7b55ee3e8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203118
Listing Expiration 2026-12-31
Marketing Start 2015-11-02

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 71205039
Hyphenated Format 71205-039

Supplemental Identifiers

RxCUI
351172
UNII
O0J6XJN02I
NUI
N0000175836 N0000000126

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 dutasteride (source: ndc)
Generic Name dutasteride (source: ndc)
Application Number ANDA203118 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (71205-039-30)
  • 60 CAPSULE in 1 BOTTLE (71205-039-60)
  • 90 CAPSULE in 1 BOTTLE (71205-039-90)
source: ndc

Packages (3)

Ingredients (1)

dutasteride (.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ca84780-9497-4cc3-a5bb-01b7b55ee3e8", "openfda": {"nui": ["N0000175836", "N0000000126"], "unii": ["O0J6XJN02I"], "rxcui": ["351172"], "spl_set_id": ["f95c3fff-1e15-4ab8-a839-6a65a5828dbb"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71205-039-30)", "package_ndc": "71205-039-30", "marketing_start_date": "20180501"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71205-039-60)", "package_ndc": "71205-039-60", "marketing_start_date": "20180501"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71205-039-90)", "package_ndc": "71205-039-90", "marketing_start_date": "20180501"}], "brand_name": "Dutasteride", "product_id": "71205-039_4ca84780-9497-4cc3-a5bb-01b7b55ee3e8", "dosage_form": "CAPSULE", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "71205-039", "generic_name": "Dutasteride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dutasteride", "active_ingredients": [{"name": "DUTASTERIDE", "strength": ".5 mg/1"}], "application_number": "ANDA203118", "marketing_category": "ANDA", "marketing_start_date": "20151102", "listing_expiration_date": "20261231"}