NDC codes

FDA NDC Directory
Product NDC (as listed)69292-540Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69292-0540Add 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
69292-540-0169292054001100 TABLET in 1 BOTTLE (69292-540-01)Marketed from Oct 15, 2025
69292-540-10692920540101000 TABLET in 1 BOTTLE (69292-540-10)Marketed from Oct 15, 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)
Enalapril Maleate
Generic name (nonproprietary)
enalapril maleate
Active ingredients
Enalapril maleate2.5 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075483
Marketing start
Listing expires
Other FDA classes
Angiotensin-converting Enzyme Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)
Identifiers
Product ID 69292-540_c55c2c6a-bb5e-4ac7-8380-6530d2f6623bSPL ID c55c2c6a-bb5e-4ac7-8380-6530d2f6623b

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

N469292054001 followed by a unit qualifier and the quantity

Package 69292-0540-01. 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 075483

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

FDA NDC Directory listings under ANDA 075483
ProductStrengthForm · routeLabelerProduct NDC
Enalapril MaleateEnalapril maleate 5 mg/1TabletOralAmici Pharma, Inc69292-542
Enalapril MaleateEnalapril maleate 10 mg/1TabletOralAmici Pharma, Inc69292-544
Enalapril MaleateEnalapril maleate 20 mg/1TabletOralAmici Pharma, Inc69292-546

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