sildenafil

Generic: sildenafil

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sildenafil
Generic Name sildenafil
Labeler chartwell rx, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sildenafil citrate 20 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-372
Product ID 62135-372_1376ad1c-0503-f5ab-e063-6394a90a0069
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202598
Listing Expiration 2026-12-31
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 62135372
Hyphenated Format 62135-372

Supplemental Identifiers

RxCUI
577033
UPC
0362135372903
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 ANDA202598 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (62135-372-90)
source: ndc

Packages (1)

62135-372-90 90 TABLET, FILM COATED in 1 BOTTLE (62135-372-90)

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": "1376ad1c-0503-f5ab-e063-6394a90a0069", "openfda": {"upc": ["0362135372903"], "unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["fcc9e04d-3507-4429-9ddd-c1fdee8acdbf"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62135-372-90)", "package_ndc": "62135-372-90", "marketing_start_date": "20240216"}], "brand_name": "Sildenafil", "product_id": "62135-372_1376ad1c-0503-f5ab-e063-6394a90a0069", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "62135-372", "generic_name": "Sildenafil", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA202598", "marketing_category": "ANDA", "marketing_start_date": "20121106", "listing_expiration_date": "20261231"}