gabapentin

Generic: gabapentin

Labeler: radha pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler radha pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

gabapentin 800 mg/1

Manufacturer
Radha Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 77771-178
Product ID 77771-178_2b2895a0-b3d1-4aa0-ac06-3b6983bdcd2d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205101
Listing Expiration 2026-12-31
Marketing Start 2023-11-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 77771178
Hyphenated Format 77771-178

Supplemental Identifiers

RxCUI
310433 310434
UPC
0377771178901 0377771177904 0377771178055
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 ANDA205101 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 800 mg/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE (77771-178-05)
  • 90 TABLET in 1 BOTTLE (77771-178-90)
source: ndc

Packages (2)

77771-178-05 500 TABLET in 1 BOTTLE (77771-178-05) 77771-178-90 90 TABLET in 1 BOTTLE (77771-178-90)

Ingredients (1)

gabapentin (800 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": "2b2895a0-b3d1-4aa0-ac06-3b6983bdcd2d", "openfda": {"nui": ["N0000008486"], "upc": ["0377771178901", "0377771177904", "0377771178055"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["1045db4e-4c76-4a0d-bf12-019bd96a8f59"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Radha Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (77771-178-05)", "package_ndc": "77771-178-05", "marketing_start_date": "20231103"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (77771-178-90)", "package_ndc": "77771-178-90", "marketing_start_date": "20231103"}], "brand_name": "Gabapentin", "product_id": "77771-178_2b2895a0-b3d1-4aa0-ac06-3b6983bdcd2d", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "77771-178", "generic_name": "Gabapentin", "labeler_name": "Radha Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA205101", "marketing_category": "ANDA", "marketing_start_date": "20231103", "listing_expiration_date": "20261231"}