sildenafil

Generic: sildenafil

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

sildenafil citrate 20 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6671
Product ID 0904-6671_93b1a3ca-d3e9-4582-8e17-d2507621675a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091479
Listing Expiration 2027-12-31
Marketing Start 2012-11-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09046671
Hyphenated Format 0904-6671

Supplemental Identifiers

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 ANDA091479 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (0904-6671-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK
  • 50 BLISTER PACK in 1 CARTON (0904-6671-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (2)

0904-6671-04 30 BLISTER PACK in 1 CARTON (0904-6671-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK 0904-6671-06 50 BLISTER PACK in 1 CARTON (0904-6671-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK

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": "93b1a3ca-d3e9-4582-8e17-d2507621675a", "openfda": {"unii": ["BW9B0ZE037"], "spl_set_id": ["a65b5fb3-ca3c-4226-9caa-42fb9a2f7373"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-6671-04)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6671-04", "marketing_start_date": "20121106"}, {"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-6671-06)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6671-06", "marketing_start_date": "20121106"}], "brand_name": "SILDENAFIL", "product_id": "0904-6671_93b1a3ca-d3e9-4582-8e17-d2507621675a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "0904-6671", "generic_name": "SILDENAFIL", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SILDENAFIL", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA091479", "marketing_category": "ANDA", "marketing_start_date": "20121106", "listing_expiration_date": "20271231"}