neurontin

Generic: gabapentin

Labeler: parke-davis div of pfizer inc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name neurontin
Generic Name gabapentin
Labeler parke-davis div of pfizer inc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

gabapentin 300 mg/1

Manufacturer
Parke-Davis Div of Pfizer Inc

Identifiers & Regulatory

Product NDC 0071-0805
Product ID 0071-0805_07bff022-5505-4611-a9a0-ce5255c339ad
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020235
Listing Expiration 2027-12-31
Marketing Start 1993-12-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00710805
Hyphenated Format 0071-0805

Supplemental Identifiers

RxCUI
105028 105029 105030 261280 261281 283523 310430 310431 310432 310433 310434 351973
UPC
0300710513242
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 NDA020235 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (0071-0805-24)
source: ndc

Packages (1)

Ingredients (1)

gabapentin (300 mg/1)

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 CAPSULE in 1 BOTTLE (0071-0805-24)", "package_ndc": "0071-0805-24", "marketing_start_date": "19931230"}], "brand_name": "Neurontin", "product_id": "0071-0805_07bff022-5505-4611-a9a0-ce5255c339ad", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "0071-0805", "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": "300 mg/1"}], "application_number": "NDA020235", "marketing_category": "NDA", "marketing_start_date": "19931230", "listing_expiration_date": "20271231"}