Package 70518-2912-2

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 70518-2912-2
Digits Only 7051829122
Product NDC 70518-2912
Description

100 POUCH in 1 BOX (70518-2912-2) / 1 TABLET in 1 POUCH (70518-2912-3)

Marketing

Marketing Status
Marketed Since 2023-03-19
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": "4ab89b95-2091-c7aa-e063-6294a90ad9ba", "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 (70518-2912-2)  / 1 TABLET in 1 POUCH (70518-2912-3)", "package_ndc": "70518-2912-2", "marketing_start_date": "20230319"}], "brand_name": "Gabapentin", "product_id": "70518-2912_4ab89b95-2091-c7aa-e063-6294a90ad9ba", "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": "20271231"}