sildenafil
Generic: sildenafil
Labeler: xlcare pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
sildenafil
Generic Name
sildenafil
Labeler
xlcare pharmaceuticals inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
sildenafil citrate 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72865-101
Product ID
72865-101_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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72865101
Hyphenated Format
72865-101
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (72865-101-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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": "30 TABLET, FILM COATED in 1 BOTTLE (72865-101-30)", "package_ndc": "72865-101-30", "marketing_start_date": "20190801"}], "brand_name": "Sildenafil", "product_id": "72865-101_f26fd1e1-7c9e-b45b-e053-2995a90a162d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "72865-101", "generic_name": "Sildenafil", "labeler_name": "XLCARE Pharmaceuticals INC.", "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": "20190801", "listing_expiration_date": "20261231"}