0480-2308
Generic: tadalafil
Labeler: teva pharmaceuticals, inc.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
source: label
Resolved Composition
Strengths
- 2.5 mg/1
Packaging
- 84746 TABLET, FILM COATED in 1 BOX (0480-2308-00)
Packages (1)
Ingredients (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"}