sildenafil

Generic: sildenafil

Labeler: xlcare pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sildenafil
Generic Name sildenafil
Labeler xlcare pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sildenafil citrate 50 mg/1

Manufacturer
XLCARE Pharmaceuticals INC.

Identifiers & Regulatory

Product NDC 72865-102
Product ID 72865-102_f26fd1e1-7c9e-b45b-e053-2995a90a162d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202659
Listing Expiration 2026-12-31
Marketing Start 2019-08-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72865102
Hyphenated Format 72865-102

Supplemental Identifiers

RxCUI
312950 314228 314229
UPC
0372865101308 0372865103302 0372865102305
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 ANDA202659 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (72865-102-01)
  • 30 TABLET, FILM COATED in 1 BOTTLE (72865-102-30)
source: ndc

Packages (2)

72865-102-01 100 TABLET, FILM COATED in 1 BOTTLE (72865-102-01) 72865-102-30 30 TABLET, FILM COATED in 1 BOTTLE (72865-102-30)

Ingredients (1)

sildenafil citrate (50 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": "f26fd1e1-7c9e-b45b-e053-2995a90a162d", "openfda": {"upc": ["0372865101308", "0372865103302", "0372865102305"], "unii": ["BW9B0ZE037"], "rxcui": ["312950", "314228", "314229"], "spl_set_id": ["ae732301-384f-43ae-80d1-5e3784fe1dca"], "manufacturer_name": ["XLCARE Pharmaceuticals INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72865-102-01)", "package_ndc": "72865-102-01", "marketing_start_date": "20190801"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72865-102-30)", "package_ndc": "72865-102-30", "marketing_start_date": "20190801"}], "brand_name": "Sildenafil", "product_id": "72865-102_f26fd1e1-7c9e-b45b-e053-2995a90a162d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "72865-102", "generic_name": "Sildenafil", "labeler_name": "XLCARE Pharmaceuticals INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "50 mg/1"}], "application_number": "ANDA202659", "marketing_category": "ANDA", "marketing_start_date": "20190801", "listing_expiration_date": "20261231"}