neurontin

Generic: gabapentin

Labeler: viatris specialty llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name neurontin
Generic Name gabapentin
Labeler viatris specialty llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

gabapentin 600 mg/1

Manufacturer
Viatris Specialty LLC

Identifiers & Regulatory

Product NDC 58151-284
Product ID 58151-284_2f08fde1-cc40-43e1-b2ea-95b44505dc19
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020882
Listing Expiration 2027-12-31
Marketing Start 2025-10-01

Pharmacologic Class

Physiologic Effect
decreased central nervous system disorganized electrical activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58151284
Hyphenated Format 58151-284

Supplemental Identifiers

RxCUI
105028 105029 105030 261280 261281 283523 310430 310431 310432 310433 310434 351973
UNII
6CW7F3G59X
NUI
N0000008486

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name neurontin (source: ndc)
Generic Name gabapentin (source: ndc)
Application Number NDA020882 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (58151-284-01)
source: ndc

Packages (1)

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

Ingredients (1)

gabapentin (600 mg/1)

Linked Drug Pages (1)

Neurontin ndc-match (0.9)

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"}