gabapentin

Generic: gabapentin

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler bryant ranch prepack
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

gabapentin 300 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2139
Product ID 72162-2139_8513f8ab-cf2a-4654-b0b3-91640b319168
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206943
Listing Expiration 2026-12-31
Marketing Start 2018-05-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622139
Hyphenated Format 72162-2139

Supplemental Identifiers

RxCUI
310431
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
  • 300 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE, PLASTIC (72162-2139-1)
  • 270 CAPSULE in 1 BOTTLE, PLASTIC (72162-2139-2)
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (72162-2139-3)
  • 500 CAPSULE in 1 BOTTLE, PLASTIC (72162-2139-5)
  • 90 CAPSULE in 1 BOTTLE, PLASTIC (72162-2139-9)
source: ndc

Packages (5)

72162-2139-1 100 CAPSULE in 1 BOTTLE, PLASTIC (72162-2139-1) 72162-2139-2 270 CAPSULE in 1 BOTTLE, PLASTIC (72162-2139-2) 72162-2139-3 30 CAPSULE in 1 BOTTLE, PLASTIC (72162-2139-3) 72162-2139-5 500 CAPSULE in 1 BOTTLE, PLASTIC (72162-2139-5) 72162-2139-9 90 CAPSULE in 1 BOTTLE, PLASTIC (72162-2139-9)

Ingredients (1)

gabapentin (300 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": "8513f8ab-cf2a-4654-b0b3-91640b319168", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310431"], "spl_set_id": ["fb0b6613-57d6-4e24-946f-f5f87c460cf0"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (72162-2139-1)", "package_ndc": "72162-2139-1", "marketing_start_date": "20231012"}, {"sample": false, "description": "270 CAPSULE in 1 BOTTLE, PLASTIC (72162-2139-2)", "package_ndc": "72162-2139-2", "marketing_start_date": "20231012"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (72162-2139-3)", "package_ndc": "72162-2139-3", "marketing_start_date": "20231012"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE, PLASTIC (72162-2139-5)", "package_ndc": "72162-2139-5", "marketing_start_date": "20231012"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (72162-2139-9)", "package_ndc": "72162-2139-9", "marketing_start_date": "20231012"}], "brand_name": "Gabapentin", "product_id": "72162-2139_8513f8ab-cf2a-4654-b0b3-91640b319168", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72162-2139", "generic_name": "Gabapentin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "300 mg/1"}], "application_number": "ANDA206943", "marketing_category": "ANDA", "marketing_start_date": "20180514", "listing_expiration_date": "20261231"}