Package 58151-284-01

Brand: neurontin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 58151-284-01
Digits Only 5815128401
Product NDC 58151-284
Product ID 58151-284_2f08fde1-cc40-43e1-b2ea-95b44505dc19
Description

100 TABLET, FILM COATED in 1 BOTTLE (58151-284-01)

Marketing

Marketing Status
Marketed Since 2025-10-01
Brand neurontin
Generic gabapentin
Sample Package No

Linked Drug Pages (1)

Neurontin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2f08fde1-cc40-43e1-b2ea-95b44505dc19", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["105028", "105029", "105030", "261280", "261281", "283523", "310430", "310431", "310432", "310433", "310434", "351973"], "spl_set_id": ["97935fd9-1d4a-43b6-a5d9-de994591187b"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Viatris Specialty LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (58151-284-01)", "package_ndc": "58151-284-01", "marketing_start_date": "20251001"}], "brand_name": "Neurontin", "product_id": "58151-284_2f08fde1-cc40-43e1-b2ea-95b44505dc19", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "58151-284", "generic_name": "gabapentin", "labeler_name": "Viatris Specialty LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Neurontin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "NDA020882", "marketing_category": "NDA", "marketing_start_date": "20251001", "listing_expiration_date": "20271231"}