sildenafil

Generic: sildenafil

Labeler: directrx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sildenafil
Generic Name sildenafil
Labeler directrx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sildenafil citrate 20 mg/1

Manufacturer
DirectRx

Identifiers & Regulatory

Product NDC 72189-298
Product ID 72189-298_2c294bda-345a-ad0e-e063-6294a90a0304
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210394
Listing Expiration 2026-12-31
Marketing Start 2021-11-29

Pharmacologic Class

Classes
phosphodiesterase 5 inhibitor [epc] phosphodiesterase 5 inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189298
Hyphenated Format 72189-298

Supplemental Identifiers

RxCUI
577033
UNII
BW9B0ZE037

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 sildenafil (source: ndc)
Generic Name sildenafil (source: ndc)
Application Number ANDA210394 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 15 TABLET in 1 BOTTLE (72189-298-15)
  • 20 TABLET in 1 BOTTLE (72189-298-20)
  • 30 TABLET in 1 BOTTLE (72189-298-30)
  • 90 TABLET in 1 BOTTLE (72189-298-90)
source: ndc

Packages (4)

Ingredients (1)

sildenafil citrate (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c294bda-345a-ad0e-e063-6294a90a0304", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["d1ee9139-13ac-7d5b-e053-2995a90a8e50"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (72189-298-15)", "package_ndc": "72189-298-15", "marketing_start_date": "20211129"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (72189-298-20)", "package_ndc": "72189-298-20", "marketing_start_date": "20211129"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-298-30)", "package_ndc": "72189-298-30", "marketing_start_date": "20220728"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-298-90)", "package_ndc": "72189-298-90", "marketing_start_date": "20211129"}], "brand_name": "SILDENAFIL", "product_id": "72189-298_2c294bda-345a-ad0e-e063-6294a90a0304", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "72189-298", "generic_name": "SILDENAFIL", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SILDENAFIL", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA210394", "marketing_category": "ANDA", "marketing_start_date": "20211129", "listing_expiration_date": "20261231"}