tadalafil
Generic: tadalafil
Labeler: nucare pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
tadalafil
Generic Name
tadalafil
Labeler
nucare pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
tadalafil 2.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-3800
Product ID
68071-3800_2eae8155-aea4-6b63-e063-6394a90a55b3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210609
Listing Expiration
2026-12-31
Marketing Start
2022-01-18
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680713800
Hyphenated Format
68071-3800
Supplemental Identifiers
RxCUI
UPC
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
ANDA210609 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2.5 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (68071-3800-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2eae8155-aea4-6b63-e063-6394a90a55b3", "openfda": {"nui": ["N0000175599", "N0000020026"], "upc": ["0368071380033"], "unii": ["742SXX0ICT"], "rxcui": ["757707"], "spl_set_id": ["2eae8756-5c7f-2545-e063-6294a90a6d52"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3800-3)", "package_ndc": "68071-3800-3", "marketing_start_date": "20250221"}], "brand_name": "TADALAFIL", "product_id": "68071-3800_2eae8155-aea4-6b63-e063-6394a90a55b3", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "68071-3800", "generic_name": "tadalafil", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TADALAFIL", "active_ingredients": [{"name": "TADALAFIL", "strength": "2.5 mg/1"}], "application_number": "ANDA210609", "marketing_category": "ANDA", "marketing_start_date": "20220118", "listing_expiration_date": "20261231"}