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, FILM COATED
Routes
ORAL
Active Ingredients

gabapentin 600 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6854
Product ID 50090-6854_38b796d8-75a7-4fef-9e33-0adaca3de95e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200651
Listing Expiration 2027-12-31
Marketing Start 2011-10-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906854
Hyphenated Format 50090-6854

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 ANDA200651 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-6854-0)
  • 60 TABLET, FILM COATED in 1 BOTTLE (50090-6854-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-6854-2)
source: ndc

Packages (3)

50090-6854-0 90 TABLET, FILM COATED in 1 BOTTLE (50090-6854-0) 50090-6854-1 60 TABLET, FILM COATED in 1 BOTTLE (50090-6854-1) 50090-6854-2 30 TABLET, FILM COATED in 1 BOTTLE (50090-6854-2)

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": "38b796d8-75a7-4fef-9e33-0adaca3de95e", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["0e1d17d5-d39c-4144-aac0-7c0d3bc9ec0d"], "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, FILM COATED in 1 BOTTLE (50090-6854-0)", "package_ndc": "50090-6854-0", "marketing_start_date": "20231130"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-6854-1)", "package_ndc": "50090-6854-1", "marketing_start_date": "20231130"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6854-2)", "package_ndc": "50090-6854-2", "marketing_start_date": "20231130"}], "brand_name": "Gabapentin", "product_id": "50090-6854_38b796d8-75a7-4fef-9e33-0adaca3de95e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-6854", "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": "ANDA200651", "marketing_category": "ANDA", "marketing_start_date": "20111006", "listing_expiration_date": "20271231"}