Aminocaproic Acid NDC 60687-739

NDC codes

FDA NDC Directory

Product NDC (as listed)60687-739Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60687-0739Add 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 NDC	11-digit (billing)	Package	Copy
60687-739-25	60687073925	30 BLISTER PACK in 1 CARTON (60687-739-25) / 1 TABLET in 1 BLISTER PACK (60687-739-95)Marketed from Mar 10, 2023

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): Aminocaproic Acid
Generic name (nonproprietary): aminocaproic acid
Active ingredients: Aminocaproic acid — 500 mg/1
Dosage form: Tablet
Route: Oral
Labeler: American Health Packaging
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 209060
Marketing start: Mar 10, 2023
Marketing end: Apr 30, 2028
Other FDA classes: Decreased Fibrinolysis (Physiologic effect)
Identifiers: Product ID 60687-739_5bffddcb-af2b-ff5d-e063-6294a90a635fSPL ID 5bffddcb-af2b-ff5d-e063-6294a90a635f
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

N460687073925 followed by a unit qualifier and the quantity

Package 60687-0739-25. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 209060

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 209060
Product	Strength	Form · route	Labeler	Product NDC
Aminocaproic Acid	Aminocaproic acid 500 mg/1	TabletOral	Vitruvias Therapeutics	69680-115
Aminocaproic Acid	Aminocaproic acid 1000 mg/1	TabletOral	Vitruvias Therapeutics	69680-116