Package 83301-0002-1
Brand: gabapentin
Generic: gabapentinPackage Facts
Identity
Package NDC
83301-0002-1
Digits Only
8330100021
Product NDC
83301-0002
Description
100 TABLET, COATED in 1 BOTTLE, PLASTIC (83301-0002-1)
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": "423fc29b-e05c-0d6b-e063-6294a90abf30", "openfda": {"nui": ["N0000008486"], "upc": ["0383301000215"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["47a22de2-ec66-45be-8648-89ed3ab6e67e"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Mullan Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE, PLASTIC (83301-0002-1)", "package_ndc": "83301-0002-1", "marketing_start_date": "20240101"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE, PLASTIC (83301-0002-2)", "package_ndc": "83301-0002-2", "marketing_start_date": "20240101"}], "brand_name": "Gabapentin", "product_id": "83301-0002_423fc29b-e05c-0d6b-e063-6294a90abf30", "dosage_form": "TABLET, COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "83301-0002", "generic_name": "Gabapentin", "labeler_name": "Mullan Pharmaceutical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA207057", "marketing_category": "ANDA", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}