sildenafil

Generic: sildenafil

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

sildenafil citrate 20 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-668
Product ID 43063-668_413a01b0-e265-c70e-e063-6394a90aac5d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078380
Marketing Start 2013-05-31
Marketing End 2026-03-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43063668
Hyphenated Format 43063-668

Supplemental Identifiers

RxCUI
577033
UPC
0343063676103
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 ANDA078380 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-668-30)
source: ndc

Packages (1)

43063-668-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-668-30)

Ingredients (1)

sildenafil citrate (20 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": "413a01b0-e265-c70e-e063-6394a90aac5d", "openfda": {"upc": ["0343063676103"], "unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["30886aaa-4834-4a06-e054-00144ff8d46c"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-668-30)", "package_ndc": "43063-668-30", "marketing_end_date": "20260331", "marketing_start_date": "20160415"}], "brand_name": "Sildenafil", "product_id": "43063-668_413a01b0-e265-c70e-e063-6394a90aac5d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "43063-668", "generic_name": "Sildenafil", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA078380", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20130531"}