Package 63629-8491-1

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 63629-8491-1
Digits Only 6362984911
Product NDC 63629-8491
Product ID 63629-8491_77d1ac6f-12ec-4a4d-99ea-e6e26f7ef1af
Description

500 TABLET in 1 BOTTLE (63629-8491-1)

Marketing

Marketing Status
Marketed Since 2016-02-04
Brand gabapentin
Generic gabapentin
Sample Package No

Linked Drug Pages (1)

Gabapentin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "77d1ac6f-12ec-4a4d-99ea-e6e26f7ef1af", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["abb56036-88df-4720-ba78-529971671545"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (63629-8491-1)", "package_ndc": "63629-8491-1", "marketing_start_date": "20160204"}], "brand_name": "Gabapentin", "product_id": "63629-8491_77d1ac6f-12ec-4a4d-99ea-e6e26f7ef1af", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "63629-8491", "generic_name": "Gabapentin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA205101", "marketing_category": "ANDA", "marketing_start_date": "20160204", "listing_expiration_date": "20261231"}