Package 59762-1576-1

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 59762-1576-1
Digits Only 5976215761
Product NDC 59762-1576
Description

1 BOTTLE in 1 CARTON (59762-1576-1) / 473 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2019-07-29
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": "7aa334e7-3c46-4680-a266-9049af3bf566", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["898715"], "spl_set_id": ["ebe34db4-816d-4f0a-adbb-826693662754"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (59762-1576-1)  / 473 mL in 1 BOTTLE", "package_ndc": "59762-1576-1", "marketing_start_date": "20190729"}], "brand_name": "Pregabalin", "product_id": "59762-1576_7aa334e7-3c46-4680-a266-9049af3bf566", "dosage_form": "SOLUTION", "product_ndc": "59762-1576", "dea_schedule": "CV", "generic_name": "Pregabalin", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "20 mg/mL"}], "application_number": "NDA022488", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20190729", "listing_expiration_date": "20261231"}