sildenafil
Generic: sildenafil
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
sildenafil
Generic Name
sildenafil
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET
Routes
Active Ingredients
sildenafil citrate 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-2602
Product ID
68071-2602_3ab073e6-dfb5-0795-e063-6294a90ab146
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210394
Listing Expiration
2026-12-31
Marketing Start
2018-05-04
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680712602
Hyphenated Format
68071-2602
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 (source: ndc)
Generic Name
sildenafil (source: ndc)
Application Number
ANDA210394 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 10 TABLET in 1 BOTTLE (68071-2602-1)
- 30 TABLET in 1 BOTTLE (68071-2602-3)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ab073e6-dfb5-0795-e063-6294a90ab146", "openfda": {"upc": ["0368071260236"], "unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["d35f8d6b-e642-78bb-e053-2995a90abb2e"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (68071-2602-1)", "package_ndc": "68071-2602-1", "marketing_start_date": "20250724"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-2602-3)", "package_ndc": "68071-2602-3", "marketing_start_date": "20211217"}], "brand_name": "Sildenafil", "product_id": "68071-2602_3ab073e6-dfb5-0795-e063-6294a90ab146", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "68071-2602", "generic_name": "Sildenafil", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA210394", "marketing_category": "ANDA", "marketing_start_date": "20180504", "listing_expiration_date": "20261231"}