Package 82868-073-30

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 82868-073-30
Digits Only 8286807330
Product NDC 82868-073
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (82868-073-30)

Marketing

Marketing Status
Marketed Since 2025-03-14
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": "471b2b01-665a-2ece-e063-6294a90aa7b3", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310431"], "spl_set_id": ["471b2d32-0cbd-aade-e063-6394a90a1696"], "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 (82868-073-30)", "package_ndc": "82868-073-30", "marketing_start_date": "20250314"}], "brand_name": "gabapentin", "product_id": "82868-073_471b2b01-665a-2ece-e063-6294a90aa7b3", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "82868-073", "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": "ANDA207099", "marketing_category": "ANDA", "marketing_start_date": "20250314", "listing_expiration_date": "20261231"}