gabapentin

Generic: gabapentin

Labeler: epic pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler epic pharma, llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

gabapentin 400 mg/1

Manufacturer
Epic Pharma, LLC

Identifiers & Regulatory

Product NDC 42806-511
Product ID 42806-511_20f2898a-4fc1-450c-a7e8-36e3d8219ee0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207099
Listing Expiration 2026-12-31
Marketing Start 2017-03-24

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42806511
Hyphenated Format 42806-511

Supplemental Identifiers

RxCUI
310430 310431 310432
UPC
0342806509302
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 gabapentin (source: ndc)
Generic Name gabapentin (source: ndc)
Application Number ANDA207099 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (42806-511-01)
  • 1000 CAPSULE in 1 BOTTLE (42806-511-10)
  • 30 CAPSULE in 1 BOTTLE (42806-511-30)
source: ndc

Packages (3)

42806-511-01 100 CAPSULE in 1 BOTTLE (42806-511-01) 42806-511-10 1000 CAPSULE in 1 BOTTLE (42806-511-10) 42806-511-30 30 CAPSULE in 1 BOTTLE (42806-511-30)

Ingredients (1)

gabapentin (400 mg/1)

Linked Drug Pages (1)

Gabapentin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "20f2898a-4fc1-450c-a7e8-36e3d8219ee0", "openfda": {"nui": ["N0000008486"], "upc": ["0342806509302"], "unii": ["6CW7F3G59X"], "rxcui": ["310430", "310431", "310432"], "spl_set_id": ["030e656a-e384-49ac-830f-32140c18112d"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (42806-511-01)", "package_ndc": "42806-511-01", "marketing_start_date": "20170324"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (42806-511-10)", "package_ndc": "42806-511-10", "marketing_start_date": "20170324"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (42806-511-30)", "package_ndc": "42806-511-30", "marketing_start_date": "20170324"}], "brand_name": "Gabapentin", "product_id": "42806-511_20f2898a-4fc1-450c-a7e8-36e3d8219ee0", "dosage_form": "CAPSULE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "42806-511", "generic_name": "Gabapentin", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "400 mg/1"}], "application_number": "ANDA207099", "marketing_category": "ANDA", "marketing_start_date": "20170324", "listing_expiration_date": "20261231"}