sildenafil

Generic: sildenafil

Labeler: avkare
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

sildenafil citrate 20 mg/1

Manufacturer
AvKARE

Identifiers & Regulatory

Product NDC 42291-937
Product ID 42291-937_48c0e47e-08b2-0c73-e063-6394a90a90b7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202025
Listing Expiration 2027-12-31
Marketing Start 2024-09-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42291937
Hyphenated Format 42291-937

Supplemental Identifiers

RxCUI
577033
UNII
BW9B0ZE037

Packaging Origin

Original Packager
true

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 ANDA202025 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (42291-937-90)
source: ndc

Packages (1)

42291-937-90 90 TABLET in 1 BOTTLE (42291-937-90)

Ingredients (1)

sildenafil citrate (20 mg/1)

Linked Drug Pages (1)

Sildenafil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "48c0e47e-08b2-0c73-e063-6394a90a90b7", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["21c83ff3-c359-3269-e063-6394a90a57ee"], "manufacturer_name": ["AvKARE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (42291-937-90)", "package_ndc": "42291-937-90", "marketing_start_date": "20240910"}], "brand_name": "Sildenafil", "product_id": "42291-937_48c0e47e-08b2-0c73-e063-6394a90a90b7", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "42291-937", "generic_name": "Sildenafil", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA202025", "marketing_category": "ANDA", "marketing_start_date": "20240910", "listing_expiration_date": "20271231"}