Package 67877-457-47

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 67877-457-47
Digits Only 6787745747
Product NDC 67877-457
Description

473 mL in 1 BOTTLE (67877-457-47)

Marketing

Marketing Status
Marketed Since 2019-07-21
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": "59a80208-5cc1-476c-a24b-296bc68e1e0d", "openfda": {"upc": ["0367877457475"], "unii": ["55JG375S6M"], "rxcui": ["898715"], "spl_set_id": ["1b731dd5-b000-4c38-bfc8-2505b076e316"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (67877-457-47)", "package_ndc": "67877-457-47", "marketing_start_date": "20190721"}], "brand_name": "Pregabalin", "product_id": "67877-457_59a80208-5cc1-476c-a24b-296bc68e1e0d", "dosage_form": "SOLUTION", "product_ndc": "67877-457", "dea_schedule": "CV", "generic_name": "Pregabalin", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "20 mg/mL"}], "application_number": "ANDA207623", "marketing_category": "ANDA", "marketing_start_date": "20190721", "listing_expiration_date": "20261231"}