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Exhibit BInstructionsPlease download this Word document (available on the Industrial Commission/Outdoor Heritage Fund Program website at http://www.nd.gov/ndic/outdoorinfopage.htm) to your computer
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How to fill out national drug code directory

01
To fill out the national drug code directory, follow these steps:
02
Collect all the required information about the drug, such as name, strength, dosage form, and package size.
03
Obtain a unique NDC number for the drug. This can be obtained from the FDA.
04
Insert the NDC number in the appropriate field in the directory.
05
Provide additional details about the drug, such as the manufacturer name, package type, and whether it is an over-the-counter or prescription drug.
06
Ensure all the information provided is accurate and up to date.
07
Submit the completed directory entry to the relevant regulatory authority for approval and inclusion in the national drug code directory.

Who needs national drug code directory?

01
The national drug code directory is needed by various entities within the healthcare industry, including:
02
- Pharmaceutical manufacturers and distributors who need to properly identify and label their products.
03
- Healthcare providers, such as doctors and pharmacists, who use the directory to verify and prescribe medications.
04
- Regulatory authorities, including the FDA, who use the directory to track and monitor drug products.
05
- Insurance companies and pharmacies who need accurate information for reimbursement and inventory management.
06
- Researchers and public health agencies who rely on the directory for data and analysis related to drug utilization and trends.
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The National Drug Code (NDC) directory is a database that serves as a universal product identifier for human drugs in the United States.
Manufacturers, repackagers, relabelers, and distributors of prescription drugs in the U.S. are required to file the National Drug Code (NDC) directory.
The NDC directory is filled out by submitting the necessary information to the FDA in a specified format.
The purpose of the NDC directory is to provide a standardized product identifier for human drugs to facilitate the exchange of product information between manufacturers, distributors, and healthcare providers.
The information reported on the NDC directory includes the product name, strength, dosage form, route of administration, and packaging size.
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