Package 70518-4532-0

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 70518-4532-0
Digits Only 7051845320
Product NDC 70518-4532
Product ID 70518-4532_4585827a-6779-2709-e063-6294a90a6830
Description

100 POUCH in 1 BOX (70518-4532-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4532-1)

Marketing

Marketing Status
Marketed Since 2025-12-07
Brand gabapentin
Generic gabapentin
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4585827a-6779-2709-e063-6294a90a6830", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["fb726cb0-d422-48dd-a8ed-adbde812b005"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-4532-0)  / 1 TABLET, FILM COATED in 1 POUCH (70518-4532-1)", "package_ndc": "70518-4532-0", "marketing_start_date": "20251207"}], "brand_name": "Gabapentin", "product_id": "70518-4532_4585827a-6779-2709-e063-6294a90a6830", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-4532", "generic_name": "Gabapentin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA217116", "marketing_category": "ANDA", "marketing_start_date": "20251207", "listing_expiration_date": "20261231"}