A Pharma NDC code is a unique 10-digit, 3-segment number assigned to each drug product. This code identifies the labeler, product, and trade package size.
Understanding the NDC Code
The National Drug Code (NDC) is a critical identifier for pharmaceuticals in the United States. It ensures that healthcare professionals and regulatory bodies can track and identify drug products accurately.
NDC Segmentation
- First Segment (Labeler Code): This segment is assigned by the Food and Drug Administration (FDA) and identifies the manufacturer, repackager, or distributor of the drug product.
- Second Segment (Product Code): This segment identifies the specific strength, dosage form, and formulation of the drug product.
- Third Segment (Package Code): This segment identifies the trade package size.
Example: A hypothetical NDC code might look like 12345-678-90, where:
- 12345 represents the labeler code.
- 678 represents the product code.
- 90 represents the package code.
Key Features of an NDC Code
- Uniqueness: Each drug product has a unique NDC code, preventing confusion and ensuring accurate tracking.
- Identification: It identifies the manufacturer, specific product, and package size.
- Regulatory Compliance: It is crucial for regulatory compliance and reporting to the FDA.
Importance of NDC Codes
- Drug Tracking: NDC codes are essential for tracking drugs throughout the supply chain.
- Medication Safety: They help ensure the correct medication is dispensed to patients, reducing the risk of medication errors.
- Inventory Management: They aid in inventory management for pharmacies, hospitals, and other healthcare facilities.
- Claims Processing: NDC codes are used in insurance claims processing for reimbursement.
- Data Analysis: They enable data analysis for drug utilization and safety studies.
In conclusion, the NDC code is a vital component of the pharmaceutical industry. It provides a standardized way to identify drug products, ensuring patient safety, compliance, and efficient supply chain management.
