tadalafil

Generic: tadalafil

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tadalafil
Generic Name tadalafil
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

tadalafil 10 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-408
Product ID 72789-408_3246ff9a-b8c3-454f-e063-6294a90abcb2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211298
Listing Expiration 2026-12-31
Marketing Start 2020-11-02

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 72789408
Hyphenated Format 72789-408

Supplemental Identifiers

RxCUI
484814
UPC
0372789408309
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 ANDA211298 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-408-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-408-90)
source: ndc

Packages (2)

72789-408-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-408-30) 72789-408-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-408-90)

Ingredients (1)

tadalafil (10 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": "3246ff9a-b8c3-454f-e063-6294a90abcb2", "openfda": {"nui": ["N0000175599", "N0000020026"], "upc": ["0372789408309"], "unii": ["742SXX0ICT"], "rxcui": ["484814"], "spl_set_id": ["828f0ee1-b9fc-4743-9394-fc086bcf5345"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-408-30)", "package_ndc": "72789-408-30", "marketing_start_date": "20240611"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-408-90)", "package_ndc": "72789-408-90", "marketing_start_date": "20240611"}], "brand_name": "Tadalafil", "product_id": "72789-408_3246ff9a-b8c3-454f-e063-6294a90abcb2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "72789-408", "generic_name": "Tadalafil", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tadalafil", "active_ingredients": [{"name": "TADALAFIL", "strength": "10 mg/1"}], "application_number": "ANDA211298", "marketing_category": "ANDA", "marketing_start_date": "20201102", "listing_expiration_date": "20261231"}