NDC codes

FDA NDC Directory
Product NDC (as listed)16571-327Labeler and product segments. Claims need a package NDC.
Product NDC at billing width16571-0327Add 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
16571-327-03165710327031657103270330 TABLET in 1 BOTTLE (16571-327-03)Marketed from Sep 20, 2026

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 — 1000 mg/1
Dosage form
Tablet
Route
Oral
Labeler
RISING PHARMA HOLDINGS, INC.NDC labeler code 16571
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213944
Marketing start
Listing expires
Other FDA classes
Decreased Fibrinolysis (Physiologic effect)
Identifiers
Product ID 16571-327_c9542474-b523-4bf0-966e-3ce9fe35a0a2SPL ID c9542474-b523-4bf0-966e-3ce9fe35a0a2
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

N416571032703 followed by a unit qualifier and the quantity

Package 16571-0327-03. 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.

About NDC 16571-327

What is NDC 16571-327?
16571-327 is the product NDC for Aminocaproic Acid, Aminocaproic acid 1000 mg/1 tablet, listed with the FDA by RISING PHARMA HOLDINGS, INC.. 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?
RISING PHARMA HOLDINGS, INC., NDC labeler code 16571. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Aminocaproic AcidAminocaproic acid 500 mg/1TabletOralRISING PHARMA HOLDINGS, INC.16571-32616571-0326-03
Aminocaproic AcidAminocaproic acid .25 g/mLSolutionOralFlorida Pharmaceutical Products, LLC71921-17571921-0175-08
Aminocaproic AcidAminocaproic acid .25 g/mLSolutionOralApozeal Pharmaceuticals Inc.83745-29483745-0294-08
Aminocaproic acidAminocaproic acid .25 g/mLSolutionOralNovadoz Pharmaceuticals LLC72205-03272205-0032-7172205-0032-72
Aminocaproic AcidAminocaproic acid .25 g/mLSolutionOralVitruvias Therapeutics69680-11469680-0114-08
Aminocaproic acidAminocaproic acid 1000 mg/1TabletOralNovadoz Pharmaceuticals LLC72205-28672205-0286-30
Aminocaproic AcidAminocaproic acid 500 mg/1TabletOralAmerican Health Packaging60687-73960687-0739-25
Aminocaproic AcidAminocaproic acid 500 mg/1TabletOralPURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS24658-79824658-0798-30
Aminocaproic AcidAminocaproic acid 1000 mg/1TabletOralPURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS24658-79924658-0799-30
Aminocaproic AcidAminocaproic acid .25 g/mLSolutionOralCamber Pharmaceuticals, Inc.31722-03531722-0035-23

All 36 Aminocaproic Acid NDCs

Other NDCs under ANDA 213944

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

FDA NDC Directory listings under ANDA 213944
ProductStrengthForm · routeLabelerProduct NDC
Aminocaproic AcidAminocaproic acid 500 mg/1TabletOralRISING PHARMA HOLDINGS, INC.16571-326

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