tadalafil

Generic: tadalafil

Labeler: qilu pharmaceutical co., ltd.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tadalafil
Generic Name tadalafil
Labeler qilu pharmaceutical co., ltd.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

tadalafil 5 mg/1

Manufacturer
Qilu Pharmaceutical Co., Ltd.

Identifiers & Regulatory

Product NDC 67184-0524
Product ID 67184-0524_3c59b310-6a02-451b-bc53-a29022509963
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210420
Listing Expiration 2026-12-31
Marketing Start 2021-11-17

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 671840524
Hyphenated Format 67184-0524

Supplemental Identifiers

RxCUI
402019 403957 484814 757707
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 tadalafil (source: ndc)
Generic Name tadalafil (source: ndc)
Application Number ANDA210420 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (67184-0524-1)
  • 2 BLISTER PACK in 1 CARTON (67184-0524-2) / 15 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (2)

67184-0524-1 30 TABLET, FILM COATED in 1 BOTTLE (67184-0524-1) 67184-0524-2 2 BLISTER PACK in 1 CARTON (67184-0524-2) / 15 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

tadalafil (5 mg/1)

Linked Drug Pages (1)

Tadalafil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3c59b310-6a02-451b-bc53-a29022509963", "openfda": {"nui": ["N0000175599", "N0000020026"], "unii": ["742SXX0ICT"], "rxcui": ["402019", "403957", "484814", "757707"], "spl_set_id": ["f295f164-78fb-4224-b319-9f20b7a453b5"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["Qilu Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (67184-0524-1)", "package_ndc": "67184-0524-1", "marketing_start_date": "20211117"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (67184-0524-2)  / 15 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "67184-0524-2", "marketing_start_date": "20211117"}], "brand_name": "Tadalafil", "product_id": "67184-0524_3c59b310-6a02-451b-bc53-a29022509963", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "67184-0524", "generic_name": "Tadalafil", "labeler_name": "Qilu Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tadalafil", "active_ingredients": [{"name": "TADALAFIL", "strength": "5 mg/1"}], "application_number": "ANDA210420", "marketing_category": "ANDA", "marketing_start_date": "20211117", "listing_expiration_date": "20261231"}