Package 72865-253-18

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 72865-253-18
Digits Only 7286525318
Product NDC 72865-253
Description

180 CAPSULE in 1 BOTTLE (72865-253-18)

Marketing

Marketing Status
Marketed Since 2021-05-10
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": "702f8307-681f-440d-9f1d-3d26141a914b", "openfda": {"nui": ["N0000008486"], "upc": ["0372865253908", "0372865252185", "0372865254905", "0372865254059", "0372865253274", "0372865253601", "0372865253182", "0372865252901", "0372865252055", "0372865254271", "0372865253304", "0372865253052", "0372865252277"], "unii": ["6CW7F3G59X"], "rxcui": ["310430", "310431", "310432"], "spl_set_id": ["618c948d-deee-44e2-98f0-e5232171dd50"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE (72865-253-05)", "package_ndc": "72865-253-05", "marketing_start_date": "20210510"}, {"sample": false, "description": "180 CAPSULE in 1 BOTTLE (72865-253-18)", "package_ndc": "72865-253-18", "marketing_start_date": "20210510"}, {"sample": false, "description": "270 CAPSULE in 1 BOTTLE (72865-253-27)", "package_ndc": "72865-253-27", "marketing_start_date": "20210510"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72865-253-30)", "package_ndc": "72865-253-30", "marketing_start_date": "20210510"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (72865-253-60)", "package_ndc": "72865-253-60", "marketing_start_date": "20210510"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (72865-253-90)", "package_ndc": "72865-253-90", "marketing_start_date": "20210510"}], "brand_name": "GABAPENTIN", "product_id": "72865-253_702f8307-681f-440d-9f1d-3d26141a914b", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72865-253", "generic_name": "gabapentin", "labeler_name": "XLCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "300 mg/1"}], "application_number": "ANDA214956", "marketing_category": "ANDA", "marketing_start_date": "20210510", "listing_expiration_date": "20261231"}