tadalafil

Generic: tadalafil

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tadalafil
Generic Name tadalafil
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

tadalafil 2.5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2363
Product ID 71335-2363_6f71e600-ca1c-4d61-9e9f-859eef56f665
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210609
Listing Expiration 2026-12-31
Marketing Start 2022-01-18

Pharmacologic Class

Established (EPC)
phosphodiesterase 5 inhibitor [epc]
Mechanism of Action
phosphodiesterase 5 inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352363
Hyphenated Format 71335-2363

Supplemental Identifiers

RxCUI
757707
UNII
742SXX0ICT
NUI
N0000175599 N0000020026

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 tadalafil (source: ndc)
Generic Name tadalafil (source: ndc)
Application Number ANDA210609 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (71335-2363-1)
  • 30 TABLET in 1 BOTTLE (71335-2363-2)
  • 10 TABLET in 1 BOTTLE (71335-2363-3)
  • 20 TABLET in 1 BOTTLE (71335-2363-4)
source: ndc

Packages (4)

Ingredients (1)

tadalafil (2.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6f71e600-ca1c-4d61-9e9f-859eef56f665", "openfda": {"nui": ["N0000175599", "N0000020026"], "unii": ["742SXX0ICT"], "rxcui": ["757707"], "spl_set_id": ["b3a58c17-f260-4125-abd1-27da00bb0719"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2363-1)", "package_ndc": "71335-2363-1", "marketing_start_date": "20240430"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2363-2)", "package_ndc": "71335-2363-2", "marketing_start_date": "20240430"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-2363-3)", "package_ndc": "71335-2363-3", "marketing_start_date": "20240430"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-2363-4)", "package_ndc": "71335-2363-4", "marketing_start_date": "20240430"}], "brand_name": "TADALAFIL", "product_id": "71335-2363_6f71e600-ca1c-4d61-9e9f-859eef56f665", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "71335-2363", "generic_name": "tadalafil", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TADALAFIL", "active_ingredients": [{"name": "TADALAFIL", "strength": "2.5 mg/1"}], "application_number": "ANDA210609", "marketing_category": "ANDA", "marketing_start_date": "20220118", "listing_expiration_date": "20261231"}