gabapentin

Generic: gabapentin

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

gabapentin 100 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-866
Product ID 23155-866_5cc5ceff-77b9-40d2-bba6-0d4af992e3f8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211314
Marketing Start 2023-06-25
Marketing End 2026-12-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155866
Hyphenated Format 23155-866

Supplemental Identifiers

RxCUI
310430 310431 310432
UPC
0323155868012 0323155867015 0323155866018
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 ANDA211314 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (23155-866-01)
  • 500 CAPSULE in 1 BOTTLE (23155-866-05)
source: ndc

Packages (2)

23155-866-01 100 CAPSULE in 1 BOTTLE (23155-866-01) 23155-866-05 500 CAPSULE in 1 BOTTLE (23155-866-05)

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": "5cc5ceff-77b9-40d2-bba6-0d4af992e3f8", "openfda": {"nui": ["N0000008486"], "upc": ["0323155868012", "0323155867015", "0323155866018"], "unii": ["6CW7F3G59X"], "rxcui": ["310430", "310431", "310432"], "spl_set_id": ["d8daa30f-1cb3-46aa-9b68-d9aa5b0a2105"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (23155-866-01)", "package_ndc": "23155-866-01", "marketing_end_date": "20261231", "marketing_start_date": "20230625"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (23155-866-05)", "package_ndc": "23155-866-05", "marketing_end_date": "20261231", "marketing_start_date": "20230625"}], "brand_name": "GABAPENTIN", "product_id": "23155-866_5cc5ceff-77b9-40d2-bba6-0d4af992e3f8", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "23155-866", "generic_name": "gabapentin", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "100 mg/1"}], "application_number": "ANDA211314", "marketing_category": "ANDA", "marketing_end_date": "20261231", "marketing_start_date": "20230625"}