cialis

Generic: tadalafil

Labeler: eli lilly and company
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name cialis
Generic Name tadalafil
Labeler eli lilly and company
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

tadalafil 5 mg/1

Manufacturer
Eli Lilly and Company

Identifiers & Regulatory

Product NDC 0002-4462
Product ID 0002-4462_b41c0258-7ebb-4b6d-855f-622cd150db75
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021368
Listing Expiration 2026-12-31
Marketing Start 2003-11-26

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 00024462
Hyphenated Format 0002-4462

Supplemental Identifiers

RxCUI
402019 402096 402097 403957 404711 484814 757707 762660
UPC
0300024462304 0300024465343 0300024463301 0300024464308
UNII
742SXX0ICT
NUI
N0000175599 N0000020026

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 cialis (source: ndc)
Generic Name tadalafil (source: ndc)
Application Number NDA021368 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (0002-4462-30)
source: ndc

Packages (1)

Ingredients (1)

tadalafil (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b41c0258-7ebb-4b6d-855f-622cd150db75", "openfda": {"nui": ["N0000175599", "N0000020026"], "upc": ["0300024462304", "0300024465343", "0300024463301", "0300024464308"], "unii": ["742SXX0ICT"], "rxcui": ["402019", "402096", "402097", "403957", "404711", "484814", "757707", "762660"], "spl_set_id": ["bcd8f8ab-81a2-4891-83db-24a0b0e25895"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["Eli Lilly and Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0002-4462-30)", "package_ndc": "0002-4462-30", "marketing_start_date": "20031126"}], "brand_name": "Cialis", "product_id": "0002-4462_b41c0258-7ebb-4b6d-855f-622cd150db75", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "0002-4462", "generic_name": "Tadalafil", "labeler_name": "Eli Lilly and Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cialis", "active_ingredients": [{"name": "TADALAFIL", "strength": "5 mg/1"}], "application_number": "NDA021368", "marketing_category": "NDA", "marketing_start_date": "20031126", "listing_expiration_date": "20261231"}