NDC codes

FDA NDC Directory
Product NDC (as listed)75907-309Labeler and product segments. Claims need a package NDC.
Product NDC at billing width75907-0309Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
75907-309-307590703093030 TABLET in 1 BOTTLE (75907-309-30)Marketed from Aug 1, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Tranexamic Acid
Generic name (nonproprietary)
tranexamic acid
Active ingredients
Tranexamic acid — 650 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218729
Marketing start
Listing expires
Other FDA classes
Decreased Fibrinolysis (Physiologic effect)
Identifiers
Product ID 75907-309_e5a52dad-e328-48f2-9182-4df46f5572efSPL ID e5a52dad-e328-48f2-9182-4df46f5572efSPL set ID e5a52dad-e328-48f2-9182-4df46f5572efRxCUI 883826UNII 6T84R30KC1UPC 0375907309304
Pharmacologic class
Antifibrinolytic Agent

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N475907030930 followed by a unit qualifier and the quantity

Package 75907-0309-30. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

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