gabapentin

Generic: gabapentin

Labeler: xlcare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler xlcare pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

gabapentin 600 mg/1

Manufacturer
XLCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72865-255
Product ID 72865-255_96acc27b-7400-480e-b79a-baa8ac3ab801
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214957
Listing Expiration 2026-12-31
Marketing Start 2021-10-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72865255
Hyphenated Format 72865-255

Supplemental Identifiers

RxCUI
310433 310434
UPC
0372865256909 0372865255056 0372865255902 0372865256053
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 ANDA214957 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE (72865-255-05)
  • 90 TABLET in 1 BOTTLE (72865-255-90)
source: ndc

Packages (2)

72865-255-05 500 TABLET in 1 BOTTLE (72865-255-05) 72865-255-90 90 TABLET in 1 BOTTLE (72865-255-90)

Ingredients (1)

gabapentin (600 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": "96acc27b-7400-480e-b79a-baa8ac3ab801", "openfda": {"nui": ["N0000008486"], "upc": ["0372865256909", "0372865255056", "0372865255902", "0372865256053"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["707ed63a-67ca-4a62-9cbe-cdeb5c4ab506"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (72865-255-05)", "package_ndc": "72865-255-05", "marketing_start_date": "20211001"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72865-255-90)", "package_ndc": "72865-255-90", "marketing_start_date": "20211001"}], "brand_name": "GABAPENTIN", "product_id": "72865-255_96acc27b-7400-480e-b79a-baa8ac3ab801", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72865-255", "generic_name": "Gabapentin", "labeler_name": "XLCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA214957", "marketing_category": "ANDA", "marketing_start_date": "20211001", "listing_expiration_date": "20261231"}