Package 62135-372-90

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 62135-372-90
Digits Only 6213537290
Product NDC 62135-372
Product ID 62135-372_1376ad1c-0503-f5ab-e063-6394a90a0069
Description

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

Marketing

Marketing Status
Marketed Since 2024-02-16
Brand sildenafil
Generic sildenafil
Sample Package No

Linked Drug Pages (1)

Sildenafil ndc-match (0.95)

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"}