tadalafil

Generic: tadalafil

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tadalafil
Generic Name tadalafil
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

tadalafil 20 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7152
Product ID 50090-7152_f875882a-3457-445d-8519-d520aef273ac
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210609
Listing Expiration 2027-12-31
Marketing Start 2022-01-18

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 500907152
Hyphenated Format 50090-7152

Supplemental Identifiers

RxCUI
402019
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 ANDA210609 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-7152-0)
  • 10 TABLET in 1 BOTTLE (50090-7152-1)
  • 90 TABLET in 1 BOTTLE (50090-7152-2)
source: ndc

Packages (3)

50090-7152-0 30 TABLET in 1 BOTTLE (50090-7152-0) 50090-7152-1 10 TABLET in 1 BOTTLE (50090-7152-1) 50090-7152-2 90 TABLET in 1 BOTTLE (50090-7152-2)

Ingredients (1)

tadalafil (20 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": "f875882a-3457-445d-8519-d520aef273ac", "openfda": {"nui": ["N0000175599", "N0000020026"], "unii": ["742SXX0ICT"], "rxcui": ["402019"], "spl_set_id": ["cd94158b-43fa-44fc-a858-0983770efa83"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7152-0)", "package_ndc": "50090-7152-0", "marketing_start_date": "20240429"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (50090-7152-1)", "package_ndc": "50090-7152-1", "marketing_start_date": "20240429"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7152-2)", "package_ndc": "50090-7152-2", "marketing_start_date": "20240429"}], "brand_name": "TADALAFIL", "product_id": "50090-7152_f875882a-3457-445d-8519-d520aef273ac", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "50090-7152", "generic_name": "tadalafil", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TADALAFIL", "active_ingredients": [{"name": "TADALAFIL", "strength": "20 mg/1"}], "application_number": "ANDA210609", "marketing_category": "ANDA", "marketing_start_date": "20220118", "listing_expiration_date": "20271231"}