Package 70518-0053-0

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 70518-0053-0
Digits Only 7051800530
Product NDC 70518-0053
Product ID 70518-0053_47e1fb94-532d-0e2a-e063-6394a90ae6a2
Description

30 CAPSULE in 1 BLISTER PACK (70518-0053-0)

Marketing

Marketing Status
Marketed Since 2016-12-12
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": "47e1fb94-532d-0e2a-e063-6394a90ae6a2", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310432"], "spl_set_id": ["896c7782-1137-454b-aaa6-28f42c7413ef"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-0053-0)", "package_ndc": "70518-0053-0", "marketing_start_date": "20161212"}], "brand_name": "Gabapentin", "product_id": "70518-0053_47e1fb94-532d-0e2a-e063-6394a90ae6a2", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-0053", "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": "ANDA090858", "marketing_category": "ANDA", "marketing_start_date": "20161212", "listing_expiration_date": "20271231"}