sildenafil

Generic: sildenafil

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

Drug Facts

Product Profile

Brand Name sildenafil
Generic Name sildenafil
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sildenafil citrate 25 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5235
Product ID 50090-5235_893aeefd-b757-4d8c-8f17-711a114c0d9b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202659
Listing Expiration 2026-12-31
Marketing Start 2018-06-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905235
Hyphenated Format 50090-5235

Supplemental Identifiers

RxCUI
314228
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 ANDA202659 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 10 TABLET, FILM COATED in 1 BOTTLE (50090-5235-0)
source: ndc

Packages (1)

Ingredients (1)

sildenafil citrate (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "893aeefd-b757-4d8c-8f17-711a114c0d9b", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["314228"], "spl_set_id": ["3145ceda-8c1e-4601-8a9d-5fc4978226d6"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (50090-5235-0)", "package_ndc": "50090-5235-0", "marketing_start_date": "20201009"}], "brand_name": "Sildenafil", "product_id": "50090-5235_893aeefd-b757-4d8c-8f17-711a114c0d9b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "50090-5235", "generic_name": "Sildenafil", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "25 mg/1"}], "application_number": "ANDA202659", "marketing_category": "ANDA", "marketing_start_date": "20180611", "listing_expiration_date": "20261231"}