sildenafil citrate

Generic: sildenafil

Labeler: ajanta pharma usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sildenafil citrate
Generic Name sildenafil
Labeler ajanta pharma usa inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sildenafil citrate 50 mg/1

Manufacturer
Ajanta Pharma USA Inc.

Identifiers & Regulatory

Product NDC 27241-068
Product ID 27241-068_693e54c2-18ce-4ef0-8b65-894bff61dd9e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206401
Listing Expiration 2026-12-31
Marketing Start 2018-10-12

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 27241068
Hyphenated Format 27241-068

Supplemental Identifiers

RxCUI
312950 314228 314229
UPC
0327241067037 0327241068034 0327241069031
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 citrate (source: ndc)
Generic Name sildenafil (source: ndc)
Application Number ANDA206401 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (27241-068-03)
  • 500 TABLET, FILM COATED in 1 BOTTLE (27241-068-05)
  • 100 TABLET, FILM COATED in 1 BOTTLE (27241-068-10)
source: ndc

Packages (3)

27241-068-03 30 TABLET, FILM COATED in 1 BOTTLE (27241-068-03) 27241-068-05 500 TABLET, FILM COATED in 1 BOTTLE (27241-068-05) 27241-068-10 100 TABLET, FILM COATED in 1 BOTTLE (27241-068-10)

Ingredients (1)

sildenafil citrate (50 mg/1)

Linked Drug Pages (1)

Sildenafil Citrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "693e54c2-18ce-4ef0-8b65-894bff61dd9e", "openfda": {"upc": ["0327241067037", "0327241068034", "0327241069031"], "unii": ["BW9B0ZE037"], "rxcui": ["312950", "314228", "314229"], "spl_set_id": ["2ccc6fa6-f8ae-4191-806f-a887244e516a"], "manufacturer_name": ["Ajanta Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (27241-068-03)", "package_ndc": "27241-068-03", "marketing_start_date": "20181012"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (27241-068-05)", "package_ndc": "27241-068-05", "marketing_start_date": "20240729"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (27241-068-10)", "package_ndc": "27241-068-10", "marketing_start_date": "20181012"}], "brand_name": "Sildenafil Citrate", "product_id": "27241-068_693e54c2-18ce-4ef0-8b65-894bff61dd9e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "27241-068", "generic_name": "Sildenafil", "labeler_name": "Ajanta Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil Citrate", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "50 mg/1"}], "application_number": "ANDA206401", "marketing_category": "ANDA", "marketing_start_date": "20181012", "listing_expiration_date": "20261231"}