Package 70518-4482-0

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 70518-4482-0
Digits Only 7051844820
Product NDC 70518-4482
Product ID 70518-4482_3f62b056-9ce7-c339-e063-6394a90aecee
Description

90 CAPSULE in 1 BOTTLE, PLASTIC (70518-4482-0)

Marketing

Marketing Status
Marketed Since 2025-09-19
Brand gabapentin
Generic gabapentin
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3f62b056-9ce7-c339-e063-6394a90aecee", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310432"], "spl_set_id": ["4a975ebe-ae0a-446a-8a3d-2ca325e28f93"], "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 (70518-4482-0)", "package_ndc": "70518-4482-0", "marketing_start_date": "20250919"}], "brand_name": "gabapentin", "product_id": "70518-4482_3f62b056-9ce7-c339-e063-6394a90aecee", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-4482", "generic_name": "gabapentin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "400 mg/1"}], "application_number": "ANDA207099", "marketing_category": "ANDA", "marketing_start_date": "20250919", "listing_expiration_date": "20261231"}