Package 70518-2616-6

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 70518-2616-6
Digits Only 7051826166
Product NDC 70518-2616
Product ID 70518-2616_4a7a5fa7-ae72-42cf-e063-6394a90a90ee
Description

60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2616-6)

Marketing

Marketing Status
Marketed Since 2025-06-18
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": "4a7a5fa7-ae72-42cf-e063-6394a90a90ee", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["7ddc7d92-9076-41cf-97ed-d9f9edc80298"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2616-6)", "package_ndc": "70518-2616-6", "marketing_start_date": "20250618"}], "brand_name": "Gabapentin", "product_id": "70518-2616_4a7a5fa7-ae72-42cf-e063-6394a90a90ee", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-2616", "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": "ANDA200651", "marketing_category": "ANDA", "marketing_start_date": "20200309", "listing_expiration_date": "20271231"}