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 100 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2005
Product ID 71335-2005_5769d849-4f27-4701-97ec-7e3ca07339d7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090007
Listing Expiration 2026-12-31
Marketing Start 2015-12-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352005
Hyphenated Format 71335-2005

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 ANDA090007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 90 CAPSULE in 1 BOTTLE (71335-2005-1)
  • 28 CAPSULE in 1 BOTTLE (71335-2005-2)
  • 30 CAPSULE in 1 BOTTLE (71335-2005-3)
  • 60 CAPSULE in 1 BOTTLE (71335-2005-4)
  • 120 CAPSULE in 1 BOTTLE (71335-2005-5)
  • 84 CAPSULE in 1 BOTTLE (71335-2005-6)
source: ndc

Packages (6)

71335-2005-1 90 CAPSULE in 1 BOTTLE (71335-2005-1) 71335-2005-2 28 CAPSULE in 1 BOTTLE (71335-2005-2) 71335-2005-3 30 CAPSULE in 1 BOTTLE (71335-2005-3) 71335-2005-4 60 CAPSULE in 1 BOTTLE (71335-2005-4) 71335-2005-5 120 CAPSULE in 1 BOTTLE (71335-2005-5) 71335-2005-6 84 CAPSULE in 1 BOTTLE (71335-2005-6)

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": "5769d849-4f27-4701-97ec-7e3ca07339d7", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310430"], "spl_set_id": ["5769d849-4f27-4701-97ec-7e3ca07339d7"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71335-2005-1)", "package_ndc": "71335-2005-1", "marketing_start_date": "20211208"}, {"sample": false, "description": "28 CAPSULE in 1 BOTTLE (71335-2005-2)", "package_ndc": "71335-2005-2", "marketing_start_date": "20241031"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71335-2005-3)", "package_ndc": "71335-2005-3", "marketing_start_date": "20220104"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71335-2005-4)", "package_ndc": "71335-2005-4", "marketing_start_date": "20241031"}, {"sample": false, "description": "120 CAPSULE in 1 BOTTLE (71335-2005-5)", "package_ndc": "71335-2005-5", "marketing_start_date": "20241031"}, {"sample": false, "description": "84 CAPSULE in 1 BOTTLE (71335-2005-6)", "package_ndc": "71335-2005-6", "marketing_start_date": "20211202"}], "brand_name": "GABAPENTIN", "product_id": "71335-2005_5769d849-4f27-4701-97ec-7e3ca07339d7", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71335-2005", "generic_name": "gabapentin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "100 mg/1"}], "application_number": "ANDA090007", "marketing_category": "ANDA", "marketing_start_date": "20151230", "listing_expiration_date": "20261231"}