NDC codes

FDA NDC Directory
Product NDC (as listed)68682-710Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68682-0710Add 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
68682-710-0168682071001100 TABLET in 1 BOTTLE (68682-710-01)Marketed from Jul 26, 1988
68682-710-10686820710101000 TABLET in 1 BOTTLE (68682-710-10)Marketed from Jul 26, 1988

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 maleate — 2.5 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
NDA authorized genericApplication NDA 018998
Marketing start
Listing expires
Other FDA classes
Angiotensin-converting Enzyme Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)
Identifiers
Product ID 68682-710_6771388d-89b3-43ec-b69e-9cebeaa2a00aSPL ID 6771388d-89b3-43ec-b69e-9cebeaa2a00aSPL set ID ebd2a62d-a704-4f8a-a104-749a5296502fRxCUI 858804, 858810, 858813, 858817UNII 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

N468682071001 followed by a unit qualifier and the quantity

Package 68682-0710-01. 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

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 018998

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

FDA NDC Directory listings under NDA 018998
ProductStrengthForm · routeLabelerProduct NDC
Enalapril MaleateEnalapril maleate 10 mg/1TabletOralProficient Rx LP71205-075
Vasotecenalapril maleateEnalapril maleate 2.5 mg/1TabletOralBausch Health US LLC0187-0140
Vasotecenalapril maleateEnalapril maleate 5 mg/1TabletOralBausch Health US LLC0187-0141
Vasotecenalapril maleateEnalapril maleate 10 mg/1TabletOralBausch Health US LLC0187-0142
Enalapril MaleateEnalapril maleate 5 mg/1TabletOralOCEANSIDE PHARMACEUTICALS68682-711
Enalapril MaleateEnalapril maleate 10 mg/1TabletOralOCEANSIDE PHARMACEUTICALS68682-712
Enalapril MaleateEnalapril maleate 20 mg/1TabletOralOCEANSIDE PHARMACEUTICALS68682-713
Vasotecenalapril maleateEnalapril maleate 20 mg/1TabletOralBausch Health US LLC0187-0143

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