Package 72189-619-72

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 72189-619-72
Digits Only 7218961972
Product NDC 72189-619
Description

120 TABLET in 1 BOTTLE (72189-619-72)

Marketing

Marketing Status
Marketed Since 2025-03-18
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": "3375e0cd-d3ed-64d5-e063-6294a90ac5e5", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["30a2ed14-dcda-f972-e063-6294a90a417c"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (72189-619-72)", "package_ndc": "72189-619-72", "marketing_start_date": "20250318"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-619-90)", "package_ndc": "72189-619-90", "marketing_start_date": "20250318"}], "brand_name": "Gabapentin", "product_id": "72189-619_3375e0cd-d3ed-64d5-e063-6294a90ac5e5", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72189-619", "generic_name": "Gabapentin", "labeler_name": "Direct_Rx", "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": "20250318", "listing_expiration_date": "20261231"}