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 50 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-103
Product ID 72789-103_4c4e9d24-ee4e-509d-e063-6394a90acedb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202659
Listing Expiration 2027-12-31
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 72789103
Hyphenated Format 72789-103

Supplemental Identifiers

RxCUI
312950
UPC
0372789103907
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
  • 50 mg/1
source: ndc
Packaging
  • 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-103-15)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-103-90)
source: ndc

Packages (2)

72789-103-15 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-103-15) 72789-103-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-103-90)

Ingredients (1)

sildenafil citrate (50 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": "4c4e9d24-ee4e-509d-e063-6394a90acedb", "openfda": {"upc": ["0372789103907"], "unii": ["BW9B0ZE037"], "rxcui": ["312950"], "spl_set_id": ["4e3034af-bee5-4df4-8beb-fbd2b510ad73"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-103-15)", "package_ndc": "72789-103-15", "marketing_start_date": "20200722"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-103-90)", "package_ndc": "72789-103-90", "marketing_start_date": "20260305"}], "brand_name": "Sildenafil", "product_id": "72789-103_4c4e9d24-ee4e-509d-e063-6394a90acedb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "72789-103", "generic_name": "Sildenafil", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "50 mg/1"}], "application_number": "ANDA202659", "marketing_category": "ANDA", "marketing_start_date": "20180611", "listing_expiration_date": "20271231"}