Package 65862-880-60

Brand: tadalafil

Generic: tadalafil
NDC Package

Package Facts

Identity

Package NDC 65862-880-60
Digits Only 6586288060
Product NDC 65862-880
Description

60 TABLET in 1 BOTTLE (65862-880-60)

Marketing

Marketing Status
Marketed Since 2019-02-05
Brand tadalafil
Generic tadalafil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0e0e7730-aefd-4208-ad81-74fc8f114a13", "openfda": {"nui": ["N0000175599", "N0000020026"], "unii": ["742SXX0ICT"], "rxcui": ["2123194"], "spl_set_id": ["a0ecc7cf-20dd-485a-b4dd-1bbc587280a7"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (65862-880-60)", "package_ndc": "65862-880-60", "marketing_start_date": "20190205"}], "brand_name": "Tadalafil", "product_id": "65862-880_0e0e7730-aefd-4208-ad81-74fc8f114a13", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "65862-880", "generic_name": "Tadalafil", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tadalafil", "active_ingredients": [{"name": "TADALAFIL", "strength": "20 mg/1"}], "application_number": "ANDA206286", "marketing_category": "ANDA", "marketing_start_date": "20190205", "listing_expiration_date": "20261231"}