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 100 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-098
Product ID 72789-098_4031d438-4491-8f2e-e063-6394a90a9510
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202659
Listing Expiration 2026-12-31
Marketing Start 2018-06-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789098
Hyphenated Format 72789-098

Supplemental Identifiers

RxCUI
314229
UPC
0372789098159
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 ANDA202659 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-098-10)
  • 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-098-15)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-098-90)
source: ndc

Packages (3)

72789-098-10 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-098-10) 72789-098-15 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-098-15) 72789-098-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-098-90)

Ingredients (1)

sildenafil citrate (100 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": "4031d438-4491-8f2e-e063-6394a90a9510", "openfda": {"upc": ["0372789098159"], "unii": ["BW9B0ZE037"], "rxcui": ["314229"], "spl_set_id": ["e1af7b6a-378e-4337-858f-85a926eec102"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-098-10)", "package_ndc": "72789-098-10", "marketing_start_date": "20200715"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-098-15)", "package_ndc": "72789-098-15", "marketing_start_date": "20200804"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-098-90)", "package_ndc": "72789-098-90", "marketing_start_date": "20240521"}], "brand_name": "Sildenafil", "product_id": "72789-098_4031d438-4491-8f2e-e063-6394a90a9510", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "72789-098", "generic_name": "Sildenafil", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "100 mg/1"}], "application_number": "ANDA202659", "marketing_category": "ANDA", "marketing_start_date": "20180611", "listing_expiration_date": "20261231"}