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 CAPSULE
Routes
ORAL
Active Ingredients

gabapentin 400 mg/1

Manufacturer
XLCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72865-254
Product ID 72865-254_702f8307-681f-440d-9f1d-3d26141a914b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214956
Listing Expiration 2026-12-31
Marketing Start 2021-05-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72865254
Hyphenated Format 72865-254

Supplemental Identifiers

RxCUI
310430 310431 310432
UPC
0372865253908 0372865252185 0372865254905 0372865254059 0372865253274 0372865253601 0372865253182 0372865252901 0372865252055 0372865254271 0372865253304 0372865253052 0372865252277
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 ANDA214956 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 500 CAPSULE in 1 BOTTLE (72865-254-05)
  • 270 CAPSULE in 1 BOTTLE (72865-254-27)
  • 90 CAPSULE in 1 BOTTLE (72865-254-90)
source: ndc

Packages (3)

72865-254-05 500 CAPSULE in 1 BOTTLE (72865-254-05) 72865-254-27 270 CAPSULE in 1 BOTTLE (72865-254-27) 72865-254-90 90 CAPSULE in 1 BOTTLE (72865-254-90)

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": "702f8307-681f-440d-9f1d-3d26141a914b", "openfda": {"nui": ["N0000008486"], "upc": ["0372865253908", "0372865252185", "0372865254905", "0372865254059", "0372865253274", "0372865253601", "0372865253182", "0372865252901", "0372865252055", "0372865254271", "0372865253304", "0372865253052", "0372865252277"], "unii": ["6CW7F3G59X"], "rxcui": ["310430", "310431", "310432"], "spl_set_id": ["618c948d-deee-44e2-98f0-e5232171dd50"], "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 CAPSULE in 1 BOTTLE (72865-254-05)", "package_ndc": "72865-254-05", "marketing_start_date": "20210510"}, {"sample": false, "description": "270 CAPSULE in 1 BOTTLE (72865-254-27)", "package_ndc": "72865-254-27", "marketing_start_date": "20210510"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (72865-254-90)", "package_ndc": "72865-254-90", "marketing_start_date": "20210510"}], "brand_name": "GABAPENTIN", "product_id": "72865-254_702f8307-681f-440d-9f1d-3d26141a914b", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72865-254", "generic_name": "gabapentin", "labeler_name": "XLCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "400 mg/1"}], "application_number": "ANDA214956", "marketing_category": "ANDA", "marketing_start_date": "20210510", "listing_expiration_date": "20261231"}