Package 65862-286-01

Brand: perindopril erbumine

Generic: perindopril erbumine
NDC Package

Package Facts

Identity

Package NDC 65862-286-01
Digits Only 6586228601
Product NDC 65862-286
Product ID 65862-286_46f1c769-2a77-4526-8303-0abc4a78d53e
Description

100 TABLET in 1 BOTTLE (65862-286-01)

Marketing

Marketing Status
Marketed Since 2009-11-10
Brand perindopril erbumine
Generic perindopril erbumine
Sample Package No

Linked Drug Pages (1)

Perindopril Erbumine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "46f1c769-2a77-4526-8303-0abc4a78d53e", "openfda": {"unii": ["1964X464OJ"], "rxcui": ["854925", "854984", "854988"], "spl_set_id": ["87768fbf-7c63-47da-8925-0316f343d6ef"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65862-286-01)", "package_ndc": "65862-286-01", "marketing_start_date": "20091110"}], "brand_name": "Perindopril Erbumine", "product_id": "65862-286_46f1c769-2a77-4526-8303-0abc4a78d53e", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "65862-286", "generic_name": "Perindopril Erbumine", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Perindopril Erbumine", "active_ingredients": [{"name": "PERINDOPRIL ERBUMINE", "strength": "2 mg/1"}], "application_number": "ANDA079070", "marketing_category": "ANDA", "marketing_start_date": "20091110", "listing_expiration_date": "20261231"}