gabapentin

Generic: gabapentin

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

gabapentin 600 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 62756-202
Product ID 62756-202_aff50a15-df39-495f-a145-0ba59660eed8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077525
Listing Expiration 2026-12-31
Marketing Start 2022-09-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62756202
Hyphenated Format 62756-202

Supplemental Identifiers

UPC
0362756204010 0362756202016 0362756138025 0362756137028 0362756139022
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 ANDA077525 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (62756-202-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (62756-202-03)
source: ndc

Packages (2)

62756-202-01 100 TABLET, FILM COATED in 1 BOTTLE (62756-202-01) 62756-202-03 500 TABLET, FILM COATED in 1 BOTTLE (62756-202-03)

Ingredients (1)

gabapentin (600 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": "aff50a15-df39-495f-a145-0ba59660eed8", "openfda": {"nui": ["N0000008486"], "upc": ["0362756204010", "0362756202016", "0362756138025", "0362756137028", "0362756139022"], "unii": ["6CW7F3G59X"], "spl_set_id": ["c9a05f0c-b5f0-422c-9d67-6d0efc921a74"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62756-202-01)", "package_ndc": "62756-202-01", "marketing_start_date": "20220901"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (62756-202-03)", "package_ndc": "62756-202-03", "marketing_start_date": "20220901"}], "brand_name": "gabapentin", "product_id": "62756-202_aff50a15-df39-495f-a145-0ba59660eed8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "62756-202", "generic_name": "gabapentin", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA077525", "marketing_category": "ANDA", "marketing_start_date": "20220901", "listing_expiration_date": "20261231"}