gabapentin

Generic: gabapentin

Labeler: asclemed usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler asclemed usa, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

gabapentin 100 mg/1

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-868
Product ID 76420-868_26246a5d-24de-ef78-e063-6394a90aff7b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214956
Listing Expiration 2026-12-31
Marketing Start 2021-05-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76420868
Hyphenated Format 76420-868

Supplemental Identifiers

RxCUI
310430 310431 310432
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 ANDA214956 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 1000 CAPSULE in 1 BOTTLE (76420-868-00)
  • 100 CAPSULE in 1 BOTTLE (76420-868-01)
  • 500 CAPSULE in 1 BOTTLE (76420-868-05)
  • 120 CAPSULE in 1 BOTTLE (76420-868-12)
  • 240 CAPSULE in 1 BOTTLE (76420-868-24)
  • 30 CAPSULE in 1 BOTTLE (76420-868-30)
  • 60 CAPSULE in 1 BOTTLE (76420-868-60)
  • 90 CAPSULE in 1 BOTTLE (76420-868-90)
source: ndc

Packages (8)

76420-868-00 1000 CAPSULE in 1 BOTTLE (76420-868-00) 76420-868-01 100 CAPSULE in 1 BOTTLE (76420-868-01) 76420-868-05 500 CAPSULE in 1 BOTTLE (76420-868-05) 76420-868-12 120 CAPSULE in 1 BOTTLE (76420-868-12) 76420-868-24 240 CAPSULE in 1 BOTTLE (76420-868-24) 76420-868-30 30 CAPSULE in 1 BOTTLE (76420-868-30) 76420-868-60 60 CAPSULE in 1 BOTTLE (76420-868-60) 76420-868-90 90 CAPSULE in 1 BOTTLE (76420-868-90)

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": "26246a5d-24de-ef78-e063-6394a90aff7b", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310430", "310431", "310432"], "spl_set_id": ["17a62334-209d-4dc1-867a-e5780196a2ca"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (76420-868-00)", "package_ndc": "76420-868-00", "marketing_start_date": "20241105"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (76420-868-01)", "package_ndc": "76420-868-01", "marketing_start_date": "20241105"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (76420-868-05)", "package_ndc": "76420-868-05", "marketing_start_date": "20241105"}, {"sample": false, "description": "120 CAPSULE in 1 BOTTLE (76420-868-12)", "package_ndc": "76420-868-12", "marketing_start_date": "20241105"}, {"sample": false, "description": "240 CAPSULE in 1 BOTTLE (76420-868-24)", "package_ndc": "76420-868-24", "marketing_start_date": "20241105"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (76420-868-30)", "package_ndc": "76420-868-30", "marketing_start_date": "20241105"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (76420-868-60)", "package_ndc": "76420-868-60", "marketing_start_date": "20241105"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (76420-868-90)", "package_ndc": "76420-868-90", "marketing_start_date": "20241105"}], "brand_name": "GABAPENTIN", "product_id": "76420-868_26246a5d-24de-ef78-e063-6394a90aff7b", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "76420-868", "generic_name": "gabapentin", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "100 mg/1"}], "application_number": "ANDA214956", "marketing_category": "ANDA", "marketing_start_date": "20210510", "listing_expiration_date": "20261231"}