NDC Compounded Drug 79926-043-11 Gabapentin

Tablet Oral

Table of Contents

    1. Compounded Product Information
    2. NDC Crossover Products Matching Gabapentin
    3. Frequently Asked Questions

Compounded Drug Product Information

NDC Product Code 79926-043
NDC Package Code 79926-043-11
11-Digit NDC Billing Format NDC Format for Billing
For insurance billing purposes the Centers for Medicare & Medicaid Services (CMS) created an 11 digit NDC derivative identifier. If the NDC Package code is less than 11 digits the code must be padded with leading zeros. The leading zeros must be added to the appropriate segment to create a 5-4-2 configuration.		 79926004311
Package Description 500 TABLET in 1 BOTTLE, PLASTIC
Product Type What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.		 Human Compounded Drug
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.		 Gabapentin
Non-Proprietary Name What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.		 Gabapentin
Substance Name What is the Substance Name?
An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.		 Gabapentin
Usage Information Product Usage Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.		 Gabapentin is used with other medications to prevent and control seizures. It is also used to relieve nerve pain following shingles (a painful rash due to herpes zoster infection) in adults. Gabapentin is known as an anticonvulsant or antiepileptic drug.
Dosage Form Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Route Name Oral - Administration to or by way of the mouth.
Marketing Category OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Code 79926
Labeler Name What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		 Wedgewood Connect, Llc
Substance Name Gabapentin
Active Ingredients Information 50 mg
Reporting Period 2021-2

NDC Crossover Products Matching Gabapentin

NDC crossover of Gabapentin with NDC 79926-043 a human compounded drug with other similar products matching the same substance name (Gabapentin) and the same administration route (oral) or dosage form (tablet).

Frequently Asked Questions

What is the NDC number assigned to Gabapentin?

Gabapentin was assigned by its manufacturer with NDC product code 79926-043. This product is a drug classified as a human compounded drug. Compounded drugs are medications created by combining or altering existing drugs to meet the specific needs of certain patients. The NDC directory only includes information about compounded drugs from facilities that choose to assign NDC numbers to their products.

Which are the NDC package codes for Gabapentin?

The NDC package code 79926-043-11 was assigned to a 500 TABLET in 1 BOTTLE, PLASTIC of gabapentin administered oral via tablet.

Who manufactures this product?

Gabapentin is manufactured by an outsourced facility and labeled by Wedgewood Connect, Llc. All compounded drugs included in the NDC directory are classified as "Outsourcing Facility Compounded Human Drug Product (Exempt from Approval Requirements)". Outsourcing facilities are a type of drug compounding facility regulated under Section 503B of the FD&C Act could be eligible for exemptions from drug registration if they meet all the conditions specified under Section 503B.

Which are the NDC crossover matchings for this product?

We found 2 matching products that have the same substance, dosage form and administration route. The matching products are manufactured by Wedgewood Connect, LLC with NDC product codes 79926-042-10 and 79926-043-10.