neurontin
Generic: gabapentin
Labeler: parke-davis div of pfizer incDrug Facts
Product Profile
Brand Name
neurontin
Generic Name
gabapentin
Labeler
parke-davis div of pfizer inc
Dosage Form
CAPSULE
Routes
Active Ingredients
gabapentin 300 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00710805
Hyphenated Format
0071-0805
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 300 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (0071-0805-24)
Packages (1)
Ingredients (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"}