sildenafil

Generic: sildenafil

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

Drug Facts

Product Profile

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

sildenafil citrate 20 mg/1

Manufacturer
Torrent Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 13668-185
Product ID 13668-185_ea9c8639-b9ab-40ea-8471-22672a155e43
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 13668185
Hyphenated Format 13668-185

Supplemental Identifiers

RxCUI
577033
UPC
0313668185300
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 ANDA091479 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE (13668-185-05)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (13668-185-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE (13668-185-30)
  • 5000 TABLET, FILM COATED in 1 BOTTLE (13668-185-51)
  • 90 TABLET, FILM COATED in 1 BOTTLE (13668-185-90)
source: ndc

Packages (5)

13668-185-05 500 TABLET, FILM COATED in 1 BOTTLE (13668-185-05) 13668-185-10 1000 TABLET, FILM COATED in 1 BOTTLE (13668-185-10) 13668-185-30 30 TABLET, FILM COATED in 1 BOTTLE (13668-185-30) 13668-185-51 5000 TABLET, FILM COATED in 1 BOTTLE (13668-185-51) 13668-185-90 90 TABLET, FILM COATED in 1 BOTTLE (13668-185-90)

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": "ea9c8639-b9ab-40ea-8471-22672a155e43", "openfda": {"upc": ["0313668185300"], "unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["1bc081f2-399d-43fa-9e0f-9f8df0118e99"], "manufacturer_name": ["Torrent Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (13668-185-05)", "package_ndc": "13668-185-05", "marketing_start_date": "20121106"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (13668-185-10)", "package_ndc": "13668-185-10", "marketing_start_date": "20241204"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (13668-185-30)", "package_ndc": "13668-185-30", "marketing_start_date": "20121106"}, {"sample": false, "description": "5000 TABLET, FILM COATED in 1 BOTTLE (13668-185-51)", "package_ndc": "13668-185-51", "marketing_start_date": "20121106"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (13668-185-90)", "package_ndc": "13668-185-90", "marketing_start_date": "20121106"}], "brand_name": "Sildenafil", "product_id": "13668-185_ea9c8639-b9ab-40ea-8471-22672a155e43", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "13668-185", "generic_name": "Sildenafil", "labeler_name": "Torrent Pharmaceuticals Limited", "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"}