Package 60219-1315-9

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 60219-1315-9
Digits Only 6021913159
Product NDC 60219-1315
Product ID 60219-1315_05638bed-2d09-47d9-8378-1265cf468389
Description

90 CAPSULE in 1 BOTTLE (60219-1315-9)

Marketing

Marketing Status
Marketed Since 2019-07-19
Brand pregabalin
Generic pregabalin
Sample Package No

Linked Drug Pages (1)

Pregabalin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "05638bed-2d09-47d9-8378-1265cf468389", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483438", "483440", "483442", "483444", "483446", "483448", "483450", "577127"], "spl_set_id": ["3099759f-cb24-40e8-b482-9388c38c73b9"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (60219-1315-9)", "package_ndc": "60219-1315-9", "marketing_start_date": "20190719"}], "brand_name": "Pregabalin", "product_id": "60219-1315_05638bed-2d09-47d9-8378-1265cf468389", "dosage_form": "CAPSULE", "product_ndc": "60219-1315", "dea_schedule": "CV", "generic_name": "Pregabalin", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "200 mg/1"}], "application_number": "ANDA209743", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20261231"}