viagra

Generic: sildenafil citrate

Labeler: viatris specialty llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name viagra
Generic Name sildenafil citrate
Labeler viatris specialty llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sildenafil citrate 50 mg/1

Manufacturer
Viatris Specialty LLC

Identifiers & Regulatory

Product NDC 58151-427
Product ID 58151-427_dcf22623-9736-40dd-8313-394101f02fdc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020895
Listing Expiration 2027-12-31
Marketing Start 2025-08-05

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58151427
Hyphenated Format 58151-427

Supplemental Identifiers

RxCUI
213269 213270 213271 312950 314228 314229
UPC
0358151426935 0358151428939 0358151427932
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 viagra (source: ndc)
Generic Name sildenafil citrate (source: ndc)
Application Number NDA020895 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (58151-427-01)
  • 30 TABLET, FILM COATED in 1 BOTTLE (58151-427-93)
source: ndc

Packages (2)

Ingredients (1)

sildenafil citrate (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "dcf22623-9736-40dd-8313-394101f02fdc", "openfda": {"upc": ["0358151426935", "0358151428939", "0358151427932"], "unii": ["BW9B0ZE037"], "rxcui": ["213269", "213270", "213271", "312950", "314228", "314229"], "spl_set_id": ["d905dc8d-917f-4ea3-a4ee-a1ecf6967d4e"], "manufacturer_name": ["Viatris Specialty LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (58151-427-01)", "package_ndc": "58151-427-01", "marketing_start_date": "20250805"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (58151-427-93)", "package_ndc": "58151-427-93", "marketing_start_date": "20260211"}], "brand_name": "Viagra", "product_id": "58151-427_dcf22623-9736-40dd-8313-394101f02fdc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "58151-427", "generic_name": "sildenafil citrate", "labeler_name": "Viatris Specialty LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Viagra", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "50 mg/1"}], "application_number": "NDA020895", "marketing_category": "NDA", "marketing_start_date": "20250805", "listing_expiration_date": "20271231"}