0480-2308

Generic: tadalafil

Labeler: teva pharmaceuticals, inc.
NDC Directory DRUG FOR FURTHER PROCESSING DRUG FOR FURTHER PROCESSING Active

Drug Facts

Product Profile

Brand Name
Generic Name tadalafil
Labeler teva pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Active Ingredients

tadalafil 2.5 mg/1

Identifiers & Regulatory

Product NDC 0480-2308
Product ID 0480-2308_5d89ba5e-f9de-44d0-9c72-9f772eae3204
Product Type DRUG FOR FURTHER PROCESSING
Marketing Category DRUG FOR FURTHER PROCESSING
Listing Expiration 2026-12-31
Marketing Start 2024-05-24

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04802308
Hyphenated Format 0480-2308

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: label)
Generic Name tadalafil (source: ndc)
Application Number ANDA205885 (source: label)
Routes
oral
source: label

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 84746 TABLET, FILM COATED in 1 BOX (0480-2308-00)
source: ndc

Packages (1)

Ingredients (1)

tadalafil (2.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "5d89ba5e-f9de-44d0-9c72-9f772eae3204", "openfda": {}, "finished": false, "packaging": [{"description": "84746 TABLET, FILM COATED in 1 BOX (0480-2308-00)", "package_ndc": "0480-2308-00", "marketing_start_date": "24-MAY-24"}], "product_id": "0480-2308_5d89ba5e-f9de-44d0-9c72-9f772eae3204", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0480-2308", "generic_name": "Tadalafil", "labeler_name": "Teva Pharmaceuticals, Inc.", "product_type": "DRUG FOR FURTHER PROCESSING", "brand_name_base": null, "active_ingredients": [{"name": "TADALAFIL", "strength": "2.5 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_start_date": "20240524", "listing_expiration_date": "20261231"}