Package 82868-074-30

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 82868-074-30
Digits Only 8286807430
Product NDC 82868-074
Product ID 82868-074_472148fa-94fb-aad6-e063-6394a90a8e5b
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (82868-074-30)

Marketing

Marketing Status
Marketed Since 2025-04-07
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": "472148fa-94fb-aad6-e063-6394a90a8e5b", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310430"], "spl_set_id": ["47214c7c-ba1b-9107-e063-6294a90a5431"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (82868-074-30)", "package_ndc": "82868-074-30", "marketing_start_date": "20250407"}], "brand_name": "GABAPENTIN", "product_id": "82868-074_472148fa-94fb-aad6-e063-6394a90a8e5b", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "82868-074", "generic_name": "gabapentin", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "100 mg/1"}], "application_number": "ANDA214956", "marketing_category": "ANDA", "marketing_start_date": "20250407", "listing_expiration_date": "20261231"}