gabapentin

Generic: gabapentin

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler direct rx
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

gabapentin 400 mg/1

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 72189-113
Product ID 72189-113_2becf606-de3d-b686-e063-6294a90afe58
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090007
Listing Expiration 2026-12-31
Marketing Start 2020-10-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189113
Hyphenated Format 72189-113

Supplemental Identifiers

RxCUI
310430 310432 310434
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 ANDA090007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (72189-113-30)
  • 60 CAPSULE in 1 BOTTLE (72189-113-60)
  • 120 CAPSULE in 1 BOTTLE (72189-113-72)
  • 90 CAPSULE in 1 BOTTLE (72189-113-90)
source: ndc

Packages (4)

72189-113-30 30 CAPSULE in 1 BOTTLE (72189-113-30) 72189-113-60 60 CAPSULE in 1 BOTTLE (72189-113-60) 72189-113-72 120 CAPSULE in 1 BOTTLE (72189-113-72) 72189-113-90 90 CAPSULE in 1 BOTTLE (72189-113-90)

Ingredients (1)

gabapentin (400 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": "2becf606-de3d-b686-e063-6294a90afe58", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310430", "310432", "310434"], "spl_set_id": ["a7e45e3f-e382-32ba-e053-2a95a90a2537"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72189-113-30)", "package_ndc": "72189-113-30", "marketing_start_date": "20201015"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (72189-113-60)", "package_ndc": "72189-113-60", "marketing_start_date": "20201015"}, {"sample": false, "description": "120 CAPSULE in 1 BOTTLE (72189-113-72)", "package_ndc": "72189-113-72", "marketing_start_date": "20201015"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (72189-113-90)", "package_ndc": "72189-113-90", "marketing_start_date": "20201015"}], "brand_name": "GABAPENTIN", "product_id": "72189-113_2becf606-de3d-b686-e063-6294a90afe58", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72189-113", "generic_name": "GABAPENTIN", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "400 mg/1"}], "application_number": "ANDA090007", "marketing_category": "ANDA", "marketing_start_date": "20201015", "listing_expiration_date": "20261231"}