tadalafil
Generic: tadalafil
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
tadalafil
Generic Name
tadalafil
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
tadalafil 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4534
Product ID
70518-4534_459adb24-a86f-3c68-e063-6394a90af8e7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209654
Listing Expiration
2026-12-31
Marketing Start
2025-12-10
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184534
Hyphenated Format
70518-4534
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA209654 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 12 TABLET in 1 BOTTLE, PLASTIC (70518-4534-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "459adb24-a86f-3c68-e063-6394a90af8e7", "openfda": {"nui": ["N0000175599", "N0000020026"], "unii": ["742SXX0ICT"], "rxcui": ["402019"], "spl_set_id": ["ad288e9d-020a-43a0-9c07-320c5c3bbc1e"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BOTTLE, PLASTIC (70518-4534-0)", "package_ndc": "70518-4534-0", "marketing_start_date": "20251210"}], "brand_name": "Tadalafil", "product_id": "70518-4534_459adb24-a86f-3c68-e063-6394a90af8e7", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "70518-4534", "generic_name": "Tadalafil", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tadalafil", "active_ingredients": [{"name": "TADALAFIL", "strength": "20 mg/1"}], "application_number": "ANDA209654", "marketing_category": "ANDA", "marketing_start_date": "20251210", "listing_expiration_date": "20261231"}