Package 72162-1531-1

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 72162-1531-1
Digits Only 7216215311
Product NDC 72162-1531
Description

100 TABLET in 1 BOTTLE (72162-1531-1)

Marketing

Marketing Status
Marketed Since 2024-02-02
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": "54dca381-45aa-4b48-8cc8-766b2a310520", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["75caca13-1432-4c0d-8d45-f029b0b2d417"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1531-1)", "package_ndc": "72162-1531-1", "marketing_start_date": "20240202"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-1531-5)", "package_ndc": "72162-1531-5", "marketing_start_date": "20240202"}], "brand_name": "Gabapentin", "product_id": "72162-1531_54dca381-45aa-4b48-8cc8-766b2a310520", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72162-1531", "generic_name": "Gabapentin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA205101", "marketing_category": "ANDA", "marketing_start_date": "20160204", "listing_expiration_date": "20261231"}