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 800 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6189
Product ID 50090-6189_293a0007-ee4b-46b0-a69e-2ff3622ddcf3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214957
Listing Expiration 2026-12-31
Marketing Start 2021-10-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906189
Hyphenated Format 50090-6189

Supplemental Identifiers

RxCUI
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 ANDA214957 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 800 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (50090-6189-0)
  • 90 TABLET in 1 BOTTLE (50090-6189-1)
  • 30 TABLET in 1 BOTTLE (50090-6189-2)
source: ndc

Packages (3)

50090-6189-0 60 TABLET in 1 BOTTLE (50090-6189-0) 50090-6189-1 90 TABLET in 1 BOTTLE (50090-6189-1) 50090-6189-2 30 TABLET in 1 BOTTLE (50090-6189-2)

Ingredients (1)

gabapentin (800 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": "293a0007-ee4b-46b0-a69e-2ff3622ddcf3", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["40bb60c0-a2f3-4e7f-b13c-028c906c4852"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-6189-0)", "package_ndc": "50090-6189-0", "marketing_start_date": "20221027"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6189-1)", "package_ndc": "50090-6189-1", "marketing_start_date": "20221027"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-6189-2)", "package_ndc": "50090-6189-2", "marketing_start_date": "20221027"}], "brand_name": "GABAPENTIN", "product_id": "50090-6189_293a0007-ee4b-46b0-a69e-2ff3622ddcf3", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-6189", "generic_name": "Gabapentin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA214957", "marketing_category": "ANDA", "marketing_start_date": "20211001", "listing_expiration_date": "20261231"}