Package 0071-0401-24

Brand: neurontin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 0071-0401-24
Digits Only 0071040124
Product NDC 0071-0401
Description

100 TABLET, FILM COATED in 1 BOTTLE (0071-0401-24)

Marketing

Marketing Status
Discontinued 2026-07-31
Brand neurontin
Generic gabapentin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "07bff022-5505-4611-a9a0-ce5255c339ad", "openfda": {"nui": ["N0000008486"], "upc": ["0300710513242"], "unii": ["6CW7F3G59X"], "rxcui": ["105028", "105029", "105030", "261280", "261281", "283523", "310430", "310431", "310432", "310433", "310434", "351973"], "spl_set_id": ["ee9ad9ed-6d9f-4ee1-9d7f-cfad438df388"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Parke-Davis Div of Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0071-0401-24)", "package_ndc": "0071-0401-24", "marketing_end_date": "20260731", "marketing_start_date": "19981009"}], "brand_name": "Neurontin", "product_id": "0071-0401_07bff022-5505-4611-a9a0-ce5255c339ad", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "0071-0401", "generic_name": "gabapentin", "labeler_name": "Parke-Davis Div of Pfizer Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Neurontin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "NDA020882", "marketing_category": "NDA", "marketing_end_date": "20260731", "marketing_start_date": "19981009"}