Package 82868-051-30

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 82868-051-30
Digits Only 8286805130
Product NDC 82868-051
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (82868-051-30)

Marketing

Marketing Status
Marketed Since 2024-06-04
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": "46dcba1e-2a35-cfd1-e063-6394a90a19ee", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310431"], "spl_set_id": ["1b44a3ab-4d06-205f-e063-6294a90af368"], "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 (82868-051-30)", "package_ndc": "82868-051-30", "marketing_start_date": "20240604"}], "brand_name": "Gabapentin", "product_id": "82868-051_46dcba1e-2a35-cfd1-e063-6394a90a19ee", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "82868-051", "generic_name": "Gabapentin", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "300 mg/1"}], "application_number": "ANDA204989", "marketing_category": "ANDA", "marketing_start_date": "20240604", "listing_expiration_date": "20261231"}