sildenafil citrate

Generic: sildenafil

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

Drug Facts

Product Profile

Brand Name sildenafil citrate
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 43063-941
Product ID 43063-941_32d712de-811b-61a5-e063-6294a90a0f30
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091448
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 43063941
Hyphenated Format 43063-941

Supplemental Identifiers

RxCUI
312950
UPC
0343063941157
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 citrate (source: ndc)
Generic Name sildenafil (source: ndc)
Application Number ANDA091448 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-941-15)
source: ndc

Packages (1)

Ingredients (1)

sildenafil citrate (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "32d712de-811b-61a5-e063-6294a90a0f30", "openfda": {"upc": ["0343063941157"], "unii": ["BW9B0ZE037"], "rxcui": ["312950"], "spl_set_id": ["78c4551c-b922-43c9-9a5a-66377ea07bc2"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-941-15)", "package_ndc": "43063-941-15", "marketing_start_date": "20190130"}], "brand_name": "SILDENAFIL CITRATE", "product_id": "43063-941_32d712de-811b-61a5-e063-6294a90a0f30", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "43063-941", "generic_name": "SILDENAFIL", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SILDENAFIL CITRATE", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "50 mg/1"}], "application_number": "ANDA091448", "marketing_category": "ANDA", "marketing_start_date": "20180611", "listing_expiration_date": "20261231"}