gabapentin

Generic: gabapentin

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

gabapentin 600 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7714
Product ID 50090-7714_1aaf4ffc-ff81-4c72-b330-a3399489f0d1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217995
Listing Expiration 2026-12-31
Marketing Start 2024-04-04

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907714
Hyphenated Format 50090-7714

Supplemental Identifiers

RxCUI
310433
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 ANDA217995 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (50090-7714-0)
  • 60 TABLET in 1 BOTTLE (50090-7714-1)
  • 30 TABLET in 1 BOTTLE (50090-7714-2)
source: ndc

Packages (3)

50090-7714-0 90 TABLET in 1 BOTTLE (50090-7714-0) 50090-7714-1 60 TABLET in 1 BOTTLE (50090-7714-1) 50090-7714-2 30 TABLET in 1 BOTTLE (50090-7714-2)

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": "1aaf4ffc-ff81-4c72-b330-a3399489f0d1", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["6e900fc4-a2b3-411f-9ab7-8dcbb97b697b"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7714-0)", "package_ndc": "50090-7714-0", "marketing_start_date": "20251015"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-7714-1)", "package_ndc": "50090-7714-1", "marketing_start_date": "20251015"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7714-2)", "package_ndc": "50090-7714-2", "marketing_start_date": "20251015"}], "brand_name": "Gabapentin", "product_id": "50090-7714_1aaf4ffc-ff81-4c72-b330-a3399489f0d1", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-7714", "generic_name": "Gabapentin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA217995", "marketing_category": "ANDA", "marketing_start_date": "20240404", "listing_expiration_date": "20261231"}