NDC Compounded Drug 71300-6632-1 Diclofenac Sodium

Gel Topical

Table of Contents

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

Compounded Drug Product Information

NDC Product Code 71300-6632
NDC Package Code 71300-6632-1
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.		 71300663201
Package Description 24 PACKET in 1 BOX > 2.5 g in 1 PACKET
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.		 Diclofenac Sodium
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.		 Diclofenac Sodium
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.		 Diclofenac Sodium
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.		 Diclofenac is used to relieve pain, swelling (inflammation), and joint stiffness caused by arthritis. Reducing these symptoms helps you do more of your normal daily activities. This medication is known as a nonsteroidal anti-inflammatory drug (NSAID). If you are treating a chronic condition such as arthritis, ask your doctor about non-drug treatments and/or using other medications to treat your pain. See also Warning section.
Dosage Form Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Route Name Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Marketing Category OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Code 71300
Labeler Name What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		 Nubratori, Inc
Substance Name Diclofenac Sodium
Active Ingredients Information 16 mg/1 g
Reporting Period 2023-1

NDC Crossover Products Matching Diclofenac Sodium

NDC crossover of Diclofenac Sodium with NDC 71300-6632 a human compounded drug with other similar products matching the same substance name (Diclofenac Sodium) and the same administration route (topical) or dosage form (gel).

Frequently Asked Questions

What is the NDC number assigned to Diclofenac Sodium?

Diclofenac Sodium was assigned by its manufacturer with NDC product code 71300-6632. 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 Diclofenac Sodium?

The NDC package code 71300-6632-1 was assigned to a 24 PACKET in 1 BOX > 2.5 g in 1 PACKET of diclofenac sodium administered topical via gel.

Who manufactures this product?

Diclofenac Sodium is manufactured by an outsourced facility and labeled by Nubratori, Inc. 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 3 matching products that have the same substance, dosage form and administration route. The matching products are manufactured by Hybrid Pharma, Nubratori, Inc and Nubratori Inc. with NDC product codes 26436-5606-1, 71300-6573-1 and 71300-6573-1.