Package 82868-094-30

Brand: sildenafil citrate

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 82868-094-30
Digits Only 8286809430
Product NDC 82868-094
Product ID 82868-094_471b787d-535b-0abe-e063-6394a90a095c
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-094-30)

Marketing

Marketing Status
Marketed Since 2025-11-26
Brand sildenafil citrate
Generic sildenafil
Sample Package No

Linked Drug Pages (1)

Sildenafil Citrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "471b787d-535b-0abe-e063-6394a90a095c", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["471b8574-cb2a-1670-e063-6394a90a2a84"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-094-30)", "package_ndc": "82868-094-30", "marketing_start_date": "20251126"}], "brand_name": "Sildenafil Citrate", "product_id": "82868-094_471b787d-535b-0abe-e063-6394a90a095c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "82868-094", "generic_name": "Sildenafil", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil Citrate", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA204883", "marketing_category": "ANDA", "marketing_start_date": "20251126", "listing_expiration_date": "20261231"}