sildenafil

Generic: sildenafil

Labeler: macleods pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sildenafil
Generic Name sildenafil
Labeler macleods pharmaceuticals limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sildenafil citrate 20 mg/1

Manufacturer
Macleods Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 33342-121
Product ID 33342-121_03d991fd-4f2c-4086-acaf-267967cff68f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203814
Marketing Start 2014-01-03
Marketing End 2027-10-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 33342121
Hyphenated Format 33342-121

Supplemental Identifiers

RxCUI
577033
UNII
BW9B0ZE037

Packaging Origin

Original Packager
true

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 ANDA203814 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (33342-121-10)
  • 10 TABLET, FILM COATED in 1 BLISTER PACK (33342-121-12)
source: ndc

Packages (2)

33342-121-10 90 TABLET, FILM COATED in 1 BOTTLE (33342-121-10) 33342-121-12 10 TABLET, FILM COATED in 1 BLISTER PACK (33342-121-12)

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": "03d991fd-4f2c-4086-acaf-267967cff68f", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["d2892f4b-f5ba-42f5-b373-310241f4efa7"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (33342-121-10)", "package_ndc": "33342-121-10", "marketing_end_date": "20271031", "marketing_start_date": "20140103"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BLISTER PACK (33342-121-12)", "package_ndc": "33342-121-12", "marketing_end_date": "20271031", "marketing_start_date": "20140103"}], "brand_name": "Sildenafil", "product_id": "33342-121_03d991fd-4f2c-4086-acaf-267967cff68f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "33342-121", "generic_name": "Sildenafil", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA203814", "marketing_category": "ANDA", "marketing_end_date": "20271031", "marketing_start_date": "20140103"}