Package 76282-707-05

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 76282-707-05
Digits Only 7628270705
Product NDC 76282-707
Product ID 76282-707_96999ce4-193e-4817-939c-900ab87fc88f
Description

500 TABLET in 1 BOTTLE (76282-707-05)

Marketing

Marketing Status
Marketed Since 2021-10-01
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": "96999ce4-193e-4817-939c-900ab87fc88f", "openfda": {"nui": ["N0000008486"], "upc": ["0376282706054", "0376282707051", "0376282707907", "0376282706900"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["a88edb00-2189-4c8d-9dd7-9fe1571775cc"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Exelan Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (76282-707-05)", "package_ndc": "76282-707-05", "marketing_start_date": "20211001"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76282-707-90)", "package_ndc": "76282-707-90", "marketing_start_date": "20211001"}], "brand_name": "GABAPENTIN", "product_id": "76282-707_96999ce4-193e-4817-939c-900ab87fc88f", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "76282-707", "generic_name": "Gabapentin", "labeler_name": "Exelan Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA214957", "marketing_category": "ANDA", "marketing_start_date": "20211001", "listing_expiration_date": "20261231"}