gabapentin
Generic: gabapentin
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
gabapentin
Generic Name
gabapentin
Labeler
proficient rx lp
Dosage Form
CAPSULE
Routes
Active Ingredients
gabapentin 300 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
82804-206
Product ID
82804-206_64a65366-8577-48f2-9f8e-0332f126d3c1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207099
Listing Expiration
2026-12-31
Marketing Start
2022-08-01
Pharmacologic Class
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82804206
Hyphenated Format
82804-206
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
gabapentin (source: ndc)
Generic Name
gabapentin (source: ndc)
Application Number
ANDA207099 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 300 mg/1
Packaging
- 90 CAPSULE in 1 BOTTLE (82804-206-90)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "64a65366-8577-48f2-9f8e-0332f126d3c1", "openfda": {"nui": ["N0000008486"], "upc": ["0382804206902"], "unii": ["6CW7F3G59X"], "rxcui": ["310431"], "spl_set_id": ["64a65366-8577-48f2-9f8e-0332f126d3c1"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (82804-206-90)", "package_ndc": "82804-206-90", "marketing_start_date": "20250312"}], "brand_name": "Gabapentin", "product_id": "82804-206_64a65366-8577-48f2-9f8e-0332f126d3c1", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "82804-206", "generic_name": "Gabapentin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "300 mg/1"}], "application_number": "ANDA207099", "marketing_category": "ANDA", "marketing_start_date": "20220801", "listing_expiration_date": "20261231"}