Package 72162-1530-1

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 72162-1530-1
Digits Only 7216215301
Product NDC 72162-1530
Description

100 TABLET in 1 BOTTLE (72162-1530-1)

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": "1ee055ab-2134-4ff8-9602-eec71f279218", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["56378630-e7a7-4981-8212-8ea703a433d8"], "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 (72162-1530-1)", "package_ndc": "72162-1530-1", "marketing_start_date": "20240202"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-1530-5)", "package_ndc": "72162-1530-5", "marketing_start_date": "20240202"}], "brand_name": "Gabapentin", "product_id": "72162-1530_1ee055ab-2134-4ff8-9602-eec71f279218", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72162-1530", "generic_name": "Gabapentin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA205101", "marketing_category": "ANDA", "marketing_start_date": "20160204", "listing_expiration_date": "20261231"}