Package 25000-183-07

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 25000-183-07
Digits Only 2500018307
Product NDC 25000-183
Product ID 25000-183_b8d46cc7-2959-411f-839c-eced90c38e92
Description

90 CAPSULE in 1 BOTTLE (25000-183-07)

Marketing

Marketing Status
Marketed Since 2022-08-01
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": "b8d46cc7-2959-411f-839c-eced90c38e92", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483438", "483440", "483442", "483444", "483446", "483448", "483450", "577127"], "spl_set_id": ["b2b81bb6-5423-4221-8a61-f70a38d6a1e9"], "manufacturer_name": ["MARKSANS PHARMA LIMITED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (25000-183-07)", "package_ndc": "25000-183-07", "marketing_start_date": "20220801"}], "brand_name": "Pregabalin", "product_id": "25000-183_b8d46cc7-2959-411f-839c-eced90c38e92", "dosage_form": "CAPSULE", "product_ndc": "25000-183", "dea_schedule": "CV", "generic_name": "Pregabalin", "labeler_name": "MARKSANS PHARMA LIMITED", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "150 mg/1"}], "application_number": "ANDA216197", "marketing_category": "ANDA", "marketing_start_date": "20220801", "listing_expiration_date": "20261231"}