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 CAPSULE
Routes
ORAL
Active Ingredients

gabapentin 100 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-3200
Product ID 50090-3200_96a7580e-bd98-4869-9981-097278189351
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090858
Listing Expiration 2026-12-31
Marketing Start 2011-01-29

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500903200
Hyphenated Format 50090-3200

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 ANDA090858 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (50090-3200-0)
  • 100 CAPSULE in 1 BOTTLE (50090-3200-1)
  • 90 CAPSULE in 1 BOTTLE (50090-3200-2)
  • 42 CAPSULE in 1 BOTTLE (50090-3200-3)
source: ndc

Packages (4)

50090-3200-0 30 CAPSULE in 1 BOTTLE (50090-3200-0) 50090-3200-1 100 CAPSULE in 1 BOTTLE (50090-3200-1) 50090-3200-2 90 CAPSULE in 1 BOTTLE (50090-3200-2) 50090-3200-3 42 CAPSULE in 1 BOTTLE (50090-3200-3)

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": "96a7580e-bd98-4869-9981-097278189351", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310430", "310431", "310432"], "spl_set_id": ["03031adf-d36b-45ec-944e-dfce5a5de91a"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-3200-0)", "package_ndc": "50090-3200-0", "marketing_start_date": "20180117"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (50090-3200-1)", "package_ndc": "50090-3200-1", "marketing_start_date": "20180105"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-3200-2)", "package_ndc": "50090-3200-2", "marketing_start_date": "20171023"}, {"sample": false, "description": "42 CAPSULE in 1 BOTTLE (50090-3200-3)", "package_ndc": "50090-3200-3", "marketing_start_date": "20240514"}], "brand_name": "Gabapentin", "product_id": "50090-3200_96a7580e-bd98-4869-9981-097278189351", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-3200", "generic_name": "Gabapentin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "100 mg/1"}], "application_number": "ANDA090858", "marketing_category": "ANDA", "marketing_start_date": "20110129", "listing_expiration_date": "20261231"}