Package 70518-4493-0

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 70518-4493-0
Digits Only 7051844930
Product NDC 70518-4493
Description

100 CAPSULE in 1 BOTTLE, PLASTIC (70518-4493-0)

Marketing

Marketing Status
Marketed Since 2025-10-08
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": "40a674f9-a64e-9c4e-e063-6394a90ac7ae", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310430"], "spl_set_id": ["fbeccab7-08aa-4da3-868f-b47a1f3d41ef"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (70518-4493-0)", "package_ndc": "70518-4493-0", "marketing_start_date": "20251008"}], "brand_name": "GABAPENTIN", "product_id": "70518-4493_40a674f9-a64e-9c4e-e063-6394a90ac7ae", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-4493", "generic_name": "gabapentin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "100 mg/1"}], "application_number": "ANDA214956", "marketing_category": "ANDA", "marketing_start_date": "20251008", "listing_expiration_date": "20261231"}