Package 71610-882-46

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 71610-882-46
Digits Only 7161088246
Product NDC 71610-882
Description

56 CAPSULE in 1 BOTTLE (71610-882-46)

Marketing

Marketing Status
Marketed Since 2025-02-24
Brand pregabalin
Generic pregabalin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "85053f33-9372-4fd6-b67b-0e7cc1b063c5", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483448"], "spl_set_id": ["b0f34220-0657-4868-ae01-014f9300f622"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "56 CAPSULE in 1 BOTTLE (71610-882-46)", "package_ndc": "71610-882-46", "marketing_start_date": "20250224"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71610-882-53)", "package_ndc": "71610-882-53", "marketing_start_date": "20250224"}], "brand_name": "Pregabalin", "product_id": "71610-882_85053f33-9372-4fd6-b67b-0e7cc1b063c5", "dosage_form": "CAPSULE", "product_ndc": "71610-882", "dea_schedule": "CV", "generic_name": "Pregabalin", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "50 mg/1"}], "application_number": "ANDA209357", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20261231"}