Package 60687-788-21

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 60687-788-21
Digits Only 6068778821
Product NDC 60687-788
Description

30 BLISTER PACK in 1 CARTON (60687-788-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-788-11)

Marketing

Marketing Status
Marketed Since 2023-11-13
Brand sildenafil
Generic sildenafil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "440822fa-ac1f-c2b6-e063-6294a90ab06a", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["f7fbfc3b-807e-4375-a6eb-8db0eaf40c9c"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (60687-788-21)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-788-11)", "package_ndc": "60687-788-21", "marketing_start_date": "20231113"}], "brand_name": "Sildenafil", "product_id": "60687-788_440822fa-ac1f-c2b6-e063-6294a90ab06a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "60687-788", "generic_name": "Sildenafil", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA203814", "marketing_category": "ANDA", "marketing_start_date": "20231113", "listing_expiration_date": "20261231"}