sildenafil citrate
Generic: sildenafil
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
sildenafil citrate
Generic Name
sildenafil
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
sildenafil citrate 50 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43063941
Hyphenated Format
43063-941
Supplemental Identifiers
RxCUI
UPC
UNII
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
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-941-15)
Packages (1)
Ingredients (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"}