Package 72162-1318-4

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 72162-1318-4
Digits Only 7216213184
Product NDC 72162-1318
Product ID 72162-1318_a80b1881-b000-4369-ba1d-74058977324f
Description

470 mL in 1 BOTTLE (72162-1318-4)

Marketing

Marketing Status
Marketed Since 2024-11-01
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": "a80b1881-b000-4369-ba1d-74058977324f", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["283523"], "spl_set_id": ["5134369d-c7f6-4569-a425-d50e5a5d694f"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "470 mL in 1 BOTTLE (72162-1318-4)", "package_ndc": "72162-1318-4", "marketing_start_date": "20241101"}], "brand_name": "Gabapentin", "product_id": "72162-1318_a80b1881-b000-4369-ba1d-74058977324f", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72162-1318", "generic_name": "gabapentin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "250 mg/5mL"}], "application_number": "ANDA076403", "marketing_category": "ANDA", "marketing_start_date": "20121001", "listing_expiration_date": "20261231"}