Package 70518-0293-0

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 70518-0293-0
Digits Only 7051802930
Product NDC 70518-0293
Description

90 CAPSULE in 1 BOTTLE, PLASTIC (70518-0293-0)

Marketing

Marketing Status
Marketed Since 2017-03-08
Brand gabapentin
Generic gabapentin
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47e6120e-271a-e930-e063-6394a90ad1f9", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310431"], "spl_set_id": ["3e633cd0-5ee8-4a05-bcfc-0a80209bf27f"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (70518-0293-0)", "package_ndc": "70518-0293-0", "marketing_start_date": "20170308"}], "brand_name": "Gabapentin", "product_id": "70518-0293_47e6120e-271a-e930-e063-6394a90ad1f9", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-0293", "generic_name": "Gabapentin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "300 mg/1"}], "application_number": "ANDA090858", "marketing_category": "ANDA", "marketing_start_date": "20170308", "listing_expiration_date": "20271231"}