Package 68382-204-10
Brand: gabapentin
Generic: gabapentinPackage Facts
Identity
Package NDC
68382-204-10
Digits Only
6838220410
Product NDC
68382-204
Description
1000 TABLET, FILM COATED in 1 BOTTLE (68382-204-10)
Marketing
Marketing Status
Brand
gabapentin
Generic
gabapentin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e85a763f-472b-492b-bf25-a30251b9b50b", "openfda": {"nui": ["N0000008486"], "upc": ["0368382204011", "0368382205018"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["310ce005-5a24-489a-b23c-d42ab6a3bfed"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68382-204-01)", "package_ndc": "68382-204-01", "marketing_start_date": "20121016"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (68382-204-05)", "package_ndc": "68382-204-05", "marketing_start_date": "20121016"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (68382-204-10)", "package_ndc": "68382-204-10", "marketing_start_date": "20121016"}], "brand_name": "Gabapentin", "product_id": "68382-204_e85a763f-472b-492b-bf25-a30251b9b50b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "68382-204", "generic_name": "Gabapentin", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA078926", "marketing_category": "ANDA", "marketing_start_date": "20121016", "listing_expiration_date": "20261231"}