NDC codes

FDA NDC Directory
Product NDC (as listed)50090-7677Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-7677Add 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
50090-7677-05009076770030 TABLET in 1 BOTTLE (50090-7677-0)Marketed from Oct 8, 2025
50090-7677-15009076770160 TABLET in 1 BOTTLE (50090-7677-1)Marketed from Oct 8, 2025
50090-7677-35009076770390 TABLET in 1 BOTTLE (50090-7677-3)Marketed from Oct 8, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 maleate — 20 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075178
Marketing start
Listing expires
Other FDA classes
Angiotensin-converting Enzyme Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)
Identifiers
Product ID 50090-7677_68698c51-6c2c-425e-a681-fbb382d79968SPL ID 68698c51-6c2c-425e-a681-fbb382d79968SPL set ID fd0a7ecc-d6a2-4e04-a14f-1ed4dacb7df3RxCUI 858810UNII 9O25354EPJ

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

N450090767700 followed by a unit qualifier and the quantity

Package 50090-7677-00. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Hypertension Enalapril maleate tablets, USP are indicated for the treatment of hypertension. Enalapril maleate tablets, USP are effective alone or in combination with other antihypertensive agents, especially thiazide-type diuretics. The blood pressure lowering effects of enalapril maleate tablets, USP and thiazides are approximately additive. Heart Failure Enalapril maleate tablets, USP are indicated for the treatment of symptomatic congestive heart failure, usually in combination with diuretics and digitalis. In these patients enalapril maleate tablets, USP improve symptoms, increase survival, and decrease the frequency of hospitalization (see CLINICAL PHARMACOLOGY, H…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 075178

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

FDA NDC Directory listings under ANDA 075178
ProductStrengthForm · routeLabelerProduct NDC
Enalapril MaleateEnalapril maleate 10 mg/1TabletOralA-S Medication Solutions50090-7678
Enalapril MaleateEnalapril maleate 2.5 mg/1TabletOralScieGen Pharmaceuticals, Inc.50228-228
Enalapril MaleateEnalapril maleate 5 mg/1TabletOralScieGen Pharmaceuticals, Inc.50228-229
Enalapril MaleateEnalapril maleate 10 mg/1TabletOralScieGen Pharmaceuticals, Inc.50228-230
Enalapril MaleateEnalapril maleate 20 mg/1TabletOralScieGen Pharmaceuticals, Inc.50228-231

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