Package 70518-2098-0

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 70518-2098-0
Digits Only 7051820980
Product NDC 70518-2098
Product ID 70518-2098_499df340-65cd-2c44-e063-6394a90a7c02
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2098-0)

Marketing

Marketing Status
Marketed Since 2019-05-22
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": "499df340-65cd-2c44-e063-6394a90a7c02", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["07c8bb17-9bd4-4fab-994d-0412205b53b4"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2098-0)", "package_ndc": "70518-2098-0", "marketing_start_date": "20190522"}], "brand_name": "Gabapentin", "product_id": "70518-2098_499df340-65cd-2c44-e063-6394a90a7c02", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-2098", "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": "ANDA203244", "marketing_category": "ANDA", "marketing_start_date": "20190522", "listing_expiration_date": "20271231"}