sildenafil

Generic: sildenafil

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

Drug Facts

Product Profile

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

sildenafil citrate 20 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680712602
Hyphenated Format 68071-2602

Supplemental Identifiers

RxCUI
577033
UPC
0368071260236
UNII
BW9B0ZE037

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE (68071-2602-1)
  • 30 TABLET in 1 BOTTLE (68071-2602-3)
source: ndc

Packages (2)

Ingredients (1)

sildenafil citrate (20 mg/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"}