finasteride

Generic: finasteride

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name finasteride
Generic Name finasteride
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

finasteride 1 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8275
Product ID 68788-8275_a4242cc3-63e0-4514-8594-e69887285baa
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207750
Listing Expiration 2027-12-31
Marketing Start 2022-10-14

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 687888275
Hyphenated Format 68788-8275

Supplemental Identifiers

RxCUI
200172
UNII
57GNO57U7G
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 finasteride (source: ndc)
Generic Name finasteride (source: ndc)
Application Number ANDA207750 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET, COATED in 1 BOTTLE (68788-8275-3)
  • 60 TABLET, COATED in 1 BOTTLE (68788-8275-6)
  • 90 TABLET, COATED in 1 BOTTLE (68788-8275-9)
source: ndc

Packages (3)

68788-8275-3 30 TABLET, COATED in 1 BOTTLE (68788-8275-3) 68788-8275-6 60 TABLET, COATED in 1 BOTTLE (68788-8275-6) 68788-8275-9 90 TABLET, COATED in 1 BOTTLE (68788-8275-9)

Ingredients (1)

finasteride (1 mg/1)

Linked Drug Pages (1)

Finasteride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a4242cc3-63e0-4514-8594-e69887285baa", "openfda": {"nui": ["N0000175836", "N0000000126"], "unii": ["57GNO57U7G"], "rxcui": ["200172"], "spl_set_id": ["b84a67d6-695e-4a7c-9b60-95e9ad18a501"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (68788-8275-3)", "package_ndc": "68788-8275-3", "marketing_start_date": "20221014"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (68788-8275-6)", "package_ndc": "68788-8275-6", "marketing_start_date": "20221014"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (68788-8275-9)", "package_ndc": "68788-8275-9", "marketing_start_date": "20221014"}], "brand_name": "Finasteride", "product_id": "68788-8275_a4242cc3-63e0-4514-8594-e69887285baa", "dosage_form": "TABLET, COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "68788-8275", "generic_name": "Finasteride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Finasteride", "active_ingredients": [{"name": "FINASTERIDE", "strength": "1 mg/1"}], "application_number": "ANDA207750", "marketing_category": "ANDA", "marketing_start_date": "20221014", "listing_expiration_date": "20271231"}