Package 72162-1531-1
Brand: gabapentin
Generic: gabapentinPackage Facts
Identity
Package NDC
72162-1531-1
Digits Only
7216215311
Product NDC
72162-1531
Description
100 TABLET in 1 BOTTLE (72162-1531-1)
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": "54dca381-45aa-4b48-8cc8-766b2a310520", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["75caca13-1432-4c0d-8d45-f029b0b2d417"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1531-1)", "package_ndc": "72162-1531-1", "marketing_start_date": "20240202"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-1531-5)", "package_ndc": "72162-1531-5", "marketing_start_date": "20240202"}], "brand_name": "Gabapentin", "product_id": "72162-1531_54dca381-45aa-4b48-8cc8-766b2a310520", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72162-1531", "generic_name": "Gabapentin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA205101", "marketing_category": "ANDA", "marketing_start_date": "20160204", "listing_expiration_date": "20261231"}