gabapentin

Generic: gabapentin

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler direct_rx
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

gabapentin 100 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-419
Product ID 72189-419_2c4d0413-c686-1d2a-e063-6394a90a00be
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206943
Listing Expiration 2026-12-31
Marketing Start 2023-02-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189419
Hyphenated Format 72189-419

Supplemental Identifiers

RxCUI
310430
UNII
6CW7F3G59X
NUI
N0000008486

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 ANDA206943 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (72189-419-30)
  • 60 CAPSULE in 1 BOTTLE (72189-419-60)
  • 120 CAPSULE in 1 BOTTLE (72189-419-72)
  • 90 CAPSULE in 1 BOTTLE (72189-419-90)
source: ndc

Packages (4)

72189-419-30 30 CAPSULE in 1 BOTTLE (72189-419-30) 72189-419-60 60 CAPSULE in 1 BOTTLE (72189-419-60) 72189-419-72 120 CAPSULE in 1 BOTTLE (72189-419-72) 72189-419-90 90 CAPSULE in 1 BOTTLE (72189-419-90)

Ingredients (1)

gabapentin (100 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": "2c4d0413-c686-1d2a-e063-6394a90a00be", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310430"], "spl_set_id": ["f40a4ee4-ae8e-769c-e053-2a95a90a344e"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72189-419-30)", "package_ndc": "72189-419-30", "marketing_start_date": "20230206"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (72189-419-60)", "package_ndc": "72189-419-60", "marketing_start_date": "20230206"}, {"sample": false, "description": "120 CAPSULE in 1 BOTTLE (72189-419-72)", "package_ndc": "72189-419-72", "marketing_start_date": "20230206"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (72189-419-90)", "package_ndc": "72189-419-90", "marketing_start_date": "20230206"}], "brand_name": "Gabapentin", "product_id": "72189-419_2c4d0413-c686-1d2a-e063-6394a90a00be", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72189-419", "generic_name": "Gabapentin", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "100 mg/1"}], "application_number": "ANDA206943", "marketing_category": "ANDA", "marketing_start_date": "20230206", "listing_expiration_date": "20261231"}