Package 65841-705-05
Brand: gabapentin
Generic: gabapentinPackage Facts
Identity
Package NDC
65841-705-05
Digits Only
6584170505
Product NDC
65841-705
Description
500 TABLET, FILM COATED in 1 BOTTLE (65841-705-05)
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": "e9f9a5e6-0454-4601-90e4-b170bb325eb6", "openfda": {"nui": ["N0000008486"], "upc": ["0365841705010"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["b033c169-4943-4ad9-ace0-7e4a1f0dc100"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65841-705-01)", "package_ndc": "65841-705-01", "marketing_start_date": "20121016"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65841-705-05)", "package_ndc": "65841-705-05", "marketing_start_date": "20121016"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65841-705-10)", "package_ndc": "65841-705-10", "marketing_start_date": "20121016"}], "brand_name": "Gabapentin", "product_id": "65841-705_e9f9a5e6-0454-4601-90e4-b170bb325eb6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "65841-705", "generic_name": "Gabapentin", "labeler_name": "Zydus Lifesciences Limited", "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"}