Package 50268-501-01

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 50268-501-01
Digits Only 5026850101
Product NDC 50268-501
Description

100 BLISTER PACK in 1 BOX (50268-501-01) / 1 CAPSULE in 1 BLISTER PACK (50268-501-11)

Marketing

Marketing Status
Marketed Since 2025-10-09
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": "40c0f60f-acca-0215-e063-6394a90adfd1", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483438", "483440", "483442", "483448", "483450"], "spl_set_id": ["40c0f658-2a0a-034b-e063-6394a90a1097"], "manufacturer_name": ["AvPAK"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX (50268-501-01)  / 1 CAPSULE in 1 BLISTER PACK (50268-501-11)", "package_ndc": "50268-501-01", "marketing_start_date": "20251009"}], "brand_name": "Pregabalin", "product_id": "50268-501_40c0f60f-acca-0215-e063-6394a90adfd1", "dosage_form": "CAPSULE", "product_ndc": "50268-501", "dea_schedule": "CV", "generic_name": "Pregabalin", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "150 mg/1"}], "application_number": "ANDA209357", "marketing_category": "ANDA", "marketing_start_date": "20251009", "listing_expiration_date": "20261231"}