sildenafil citrate
Generic: sildenafil
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
sildenafil citrate
Generic Name
sildenafil
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
sildenafil citrate 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-3410
Product ID
68071-3410_2d6c6bd0-3323-06df-e063-6394a90af2df
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206401
Listing Expiration
2026-12-31
Marketing Start
2018-10-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680713410
Hyphenated Format
68071-3410
Supplemental Identifiers
RxCUI
UPC
UNII
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 citrate (source: ndc)
Generic Name
sildenafil (source: ndc)
Application Number
ANDA206401 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (68071-3410-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d6c6bd0-3323-06df-e063-6394a90af2df", "openfda": {"upc": ["0368071341034"], "unii": ["BW9B0ZE037"], "rxcui": ["314229"], "spl_set_id": ["fbe75c2c-0aff-9ade-e053-6394a90a1ea4"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3410-3)", "package_ndc": "68071-3410-3", "marketing_start_date": "20230518"}], "brand_name": "Sildenafil Citrate", "product_id": "68071-3410_2d6c6bd0-3323-06df-e063-6394a90af2df", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "68071-3410", "generic_name": "Sildenafil", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil Citrate", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "100 mg/1"}], "application_number": "ANDA206401", "marketing_category": "ANDA", "marketing_start_date": "20181012", "listing_expiration_date": "20261231"}