gabarone

Generic: gabapentin

Labeler: ina pharmaceutics inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabarone
Generic Name gabapentin
Labeler ina pharmaceutics inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

gabapentin 400 mg/1

Manufacturer
INA Pharmaceutics Inc.

Identifiers & Regulatory

Product NDC 74157-111
Product ID 74157-111_47d9ab92-3736-01a7-e063-6394a90a7c55
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211313
Listing Expiration 2027-12-31
Marketing Start 2024-12-23

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 74157111
Hyphenated Format 74157-111

Supplemental Identifiers

RxCUI
476673 476679 602399 602407
UPC
0374157013900 0374157111903
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 gabarone (source: ndc)
Generic Name gabapentin (source: ndc)
Application Number ANDA211313 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (74157-111-90)
source: ndc

Packages (1)

74157-111-90 90 TABLET in 1 BOTTLE (74157-111-90)

Ingredients (1)

gabapentin (400 mg/1)

Linked Drug Pages (1)

GABARONE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47d9ab92-3736-01a7-e063-6394a90a7c55", "openfda": {"nui": ["N0000008486"], "upc": ["0374157013900", "0374157111903"], "unii": ["6CW7F3G59X"], "rxcui": ["476673", "476679", "602399", "602407"], "spl_set_id": ["0f350a4b-f294-4b98-b69f-3cc789e930ba"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["INA Pharmaceutics Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (74157-111-90)", "package_ndc": "74157-111-90", "marketing_start_date": "20241223"}], "brand_name": "GABARONE", "product_id": "74157-111_47d9ab92-3736-01a7-e063-6394a90a7c55", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "74157-111", "generic_name": "Gabapentin", "labeler_name": "INA Pharmaceutics Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABARONE", "active_ingredients": [{"name": "GABAPENTIN", "strength": "400 mg/1"}], "application_number": "ANDA211313", "marketing_category": "ANDA", "marketing_start_date": "20241223", "listing_expiration_date": "20271231"}