Package 72189-069-30

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 72189-069-30
Digits Only 7218906930
Product NDC 72189-069
Description

30 TABLET, FILM COATED in 1 BOTTLE (72189-069-30)

Marketing

Marketing Status
Marketed Since 2020-06-17
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": "2be7ed74-ac68-c313-e063-6294a90ad14c", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["314229"], "spl_set_id": ["a84a418a-155c-7be7-e053-2995a90a8158"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (72189-069-10)", "package_ndc": "72189-069-10", "marketing_start_date": "20200617"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-069-30)", "package_ndc": "72189-069-30", "marketing_start_date": "20200617"}], "brand_name": "SILDENAFIL", "product_id": "72189-069_2be7ed74-ac68-c313-e063-6294a90ad14c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "72189-069", "generic_name": "SILDENAFIL", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SILDENAFIL", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "100 mg/1"}], "application_number": "ANDA202659", "marketing_category": "ANDA", "marketing_start_date": "20200617", "listing_expiration_date": "20261231"}