Package 70518-2912-0

Brand: Gabapentin

Generic: Gabapentin
NDC Package

Package Facts

Identity

Package NDC 70518-2912-0
Digits Only 7051829120
Product NDC 70518-2912
Product ID 70518-2912_3dd1e7cf-d615-675f-e063-6394a90ad3e0
Description

100 POUCH in 1 BOX (70518-2912-0) / 1 TABLET in 1 POUCH (70518-2912-1)

Marketing

Marketing Status
Marketed Since 2020-10-20
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": "3dd1e7cf-d615-675f-e063-6394a90ad3e0", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["bc525ae4-9843-4038-a1b7-0d3543e2282c"], "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 (70518-2912-0)  / 1 TABLET in 1 POUCH (70518-2912-1)", "package_ndc": "70518-2912-0", "marketing_start_date": "20201020"}, {"sample": false, "description": "100 POUCH in 1 BOX (70518-2912-2)  / 1 TABLET in 1 POUCH (70518-2912-3)", "package_ndc": "70518-2912-2", "marketing_start_date": "20230319"}], "brand_name": "Gabapentin", "product_id": "70518-2912_3dd1e7cf-d615-675f-e063-6394a90ad3e0", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-2912", "generic_name": "Gabapentin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA206402", "marketing_category": "ANDA", "marketing_start_date": "20201020", "listing_expiration_date": "20261231"}