Package 70518-4411-0

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 70518-4411-0
Digits Only 7051844110
Product NDC 70518-4411
Product ID 70518-4411_3b24724a-e8bf-1031-e063-6394a90a703c
Description

90 CAPSULE in 1 BOTTLE, PLASTIC (70518-4411-0)

Marketing

Marketing Status
Marketed Since 2025-07-30
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": "3b24724a-e8bf-1031-e063-6394a90a703c", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310431"], "spl_set_id": ["167d8b87-506c-4293-9579-563feaa71583"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (70518-4411-0)", "package_ndc": "70518-4411-0", "marketing_start_date": "20250730"}], "brand_name": "Gabapentin", "product_id": "70518-4411_3b24724a-e8bf-1031-e063-6394a90a703c", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-4411", "generic_name": "Gabapentin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "300 mg/1"}], "application_number": "ANDA206943", "marketing_category": "ANDA", "marketing_start_date": "20250730", "listing_expiration_date": "20261231"}