What is NDC 71921-175?

71921-175 is the product NDC for Aminocaproic Acid, Aminocaproic acid .25 g/mL solution, listed with the FDA by Florida Pharmaceutical Products, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Florida Pharmaceutical Products, LLC, NDC labeler code 71921. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Aminocaproic Acid?

35 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Aminocaproic Acid NDC 71921-175 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71921-175Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71921-0175Add 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
71921-175-08	71921017508	236.5 mL in 1 BOTTLE (71921-175-08)Marketed from Dec 20, 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): Aminocaproic Acid
Generic name (nonproprietary): aminocaproic acid
Active ingredients: Aminocaproic acid — .25 g/mL
Dosage form: Solution
Route: Oral
Labeler: Florida Pharmaceutical Products, LLCNDC labeler code 71921
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 215510
Marketing start: Dec 20, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Decreased Fibrinolysis (Physiologic effect)
Identifiers: Product ID 71921-175_828568a7-1808-4330-b466-01889b2311a2SPL ID 828568a7-1808-4330-b466-01889b2311a2SPL set ID 828568a7-1808-4330-b466-01889b2311a2RxCUI 582299UNII U6F3787206UPC 0371921175086
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

N471921017508 followed by a unit qualifier and the quantity

Package 71921-0175-08. 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

Current FDA label (SPL), effective Dec 20, 2025.

Indications (excerpt from the label)

INDICATIONS & USAGE Aminocaproic acid oral solution is useful in enhancing hemostasis when fibrinolysis contributes to bleeding. In life-threatening situations, transfusion of appropriate blood products and other emergency measures may be required. Fibrinolytic bleeding may frequently be associated with surgical complications following heart surgery (with or without cardiac bypass procedures) and portacaval shunt; hematological disorders such as amegakaryocytic thrombocytopenia (accompanying aplastic anemia); acute and life-threatening abruptio placentae; hepatic cirrhosis; and neoplastic disease such as carcinoma of the prostate, lung, stomach, and cervix. Urinary fibrinolysis, usually a no…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71921-175

What is NDC 71921-175?: 71921-175 is the product NDC for Aminocaproic Acid, Aminocaproic acid .25 g/mL solution, listed with the FDA by Florida Pharmaceutical Products, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Aminocaproic Acid.
What is the active ingredient?: Aminocaproic acid.
Who is the labeler?: Florida Pharmaceutical Products, LLC, NDC labeler code 71921. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Aminocaproic Acid?: 35 other product NDCs are listed under this name. See all Aminocaproic Acid NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Aminocaproic Acid NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Aminocaproic Acid	Aminocaproic acid 500 mg/1	TabletOral	RISING PHARMA HOLDINGS, INC.	16571-326	16571-0326-03
Aminocaproic Acid	Aminocaproic acid 1000 mg/1	TabletOral	RISING PHARMA HOLDINGS, INC.	16571-327	16571-0327-03
Aminocaproic Acid	Aminocaproic acid .25 g/mL	SolutionOral	Apozeal Pharmaceuticals Inc.	83745-294	83745-0294-08
Aminocaproic acid	Aminocaproic acid .25 g/mL	SolutionOral	Novadoz Pharmaceuticals LLC	72205-032	72205-0032-7172205-0032-72
Aminocaproic Acid	Aminocaproic acid .25 g/mL	SolutionOral	Vitruvias Therapeutics	69680-114	69680-0114-08
Aminocaproic acid	Aminocaproic acid 1000 mg/1	TabletOral	Novadoz Pharmaceuticals LLC	72205-286	72205-0286-30
Aminocaproic Acid	Aminocaproic acid 500 mg/1	TabletOral	American Health Packaging	60687-739	60687-0739-25
Aminocaproic Acid	Aminocaproic acid 500 mg/1	TabletOral	PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS	24658-798	24658-0798-30
Aminocaproic Acid	Aminocaproic acid 1000 mg/1	TabletOral	PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS	24658-799	24658-0799-30
Aminocaproic Acid	Aminocaproic acid .25 g/mL	SolutionOral	Camber Pharmaceuticals, Inc.	31722-035	31722-0035-23

All 36 Aminocaproic Acid NDCs