What is NDC 71205-075?

71205-075 is the product NDC for Enalapril Maleate, Enalapril maleate 10 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 3 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Enalapril Maleate?

97 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Enalapril Maleate NDC 71205-075 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71205-075Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71205-0075Add 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
71205-075-30	7120500753071205007530	30 TABLET in 1 BOTTLE (71205-075-30)Marketed from Jul 2, 2018
71205-075-60	7120500756071205007560	60 TABLET in 1 BOTTLE (71205-075-60)Marketed from Jul 2, 2018
71205-075-90	7120500759071205007590	90 TABLET in 1 BOTTLE (71205-075-90)Marketed from Jul 2, 2018

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 — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Proficient Rx LPNDC labeler code 71205
Product type: Prescription drug
Marketing category: NDA authorized genericApplication NDA 018998
Marketing start: Dec 24, 1985
Listing expires: Dec 31, 2027
Other FDA classes: Angiotensin-converting Enzyme Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)
Identifiers: Product ID 71205-075_bdfcb7c8-7269-46a6-aff8-d73b093ee88aSPL ID bdfcb7c8-7269-46a6-aff8-d73b093ee88aSPL set ID cc921315-8da1-487c-ba19-433470f5c8d8RxCUI 858817UNII 9O25354EPJ
Pharmacologic class: Angiotensin Converting Enzyme Inhibitor

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

N471205007530 followed by a unit qualifier and the quantity

Package 71205-0075-30. 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 Oct 1, 2019. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Hypertension Enalapril maleate tablet is indicated for the treatment of hypertension. Enalapril maleate tablet is 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 tablet is indicated for the treatment of symptomatic congestive heart failure, usually in combination with diuretics and digitalis. In these patients enalapril maleate tablet improves symptoms, increases survival, and decreases the frequency of hospitalization (see CLINICAL PHARMACOLOGY , Heart Failure, Mortality Tria…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71205-075

What is NDC 71205-075?: 71205-075 is the product NDC for Enalapril Maleate, Enalapril maleate 10 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Enalapril Maleate.
What is the active ingredient?: Enalapril maleate.
Who is the labeler?: Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Enalapril Maleate?: 97 other product NDCs are listed under this name. See all Enalapril Maleate 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 Enalapril Maleate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Enalapril Maleate	Enalapril maleate 2.5 mg/1	TabletOral	Coupler LLC	67046-1254	67046-1254-03
Enalapril Maleate	Enalapril maleate 5 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4164	68788-4164-0168788-4164-0368788-4164-06+1 more
Enalapril Maleate	Enalapril maleate 20 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4147	68788-4147-0068788-4147-0368788-4147-06+1 more
Enalapril Maleate	Enalapril maleate 10 mg/1	TabletOral	Coupler LLC	67046-0798	67046-0798-03
Enalapril Maleate	Enalapril maleate 10 mg/1	TabletOral	Amici Pharma, Inc	69292-544	69292-0544-0169292-0544-1069292-0544-50
Enalapril Maleate	Enalapril maleate 2.5 mg/1	TabletOral	Amici Pharma, Inc	69292-540	69292-0540-0169292-0540-10
Enalapril Maleate	Enalapril maleate 5 mg/1	TabletOral	Amici Pharma, Inc	69292-542	69292-0542-0169292-0542-1069292-0542-50
Enalapril Maleate	Enalapril maleate 20 mg/1	TabletOral	Amici Pharma, Inc	69292-546	69292-0546-0169292-0546-10
Enalapril maleate	Enalapril maleate 2.5 mg/1	TabletOral	Major Pharmaceuticals	0904-7309	00904-7309-61
Enalapril maleate	Enalapril maleate 5 mg/1	TabletOral	Major Pharmaceuticals	0904-7310	00904-7310-61

All 98 Enalapril Maleate NDCs

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
Product	Strength	Form · route	Labeler	Product NDC
Enalapril Maleate	Enalapril maleate 2.5 mg/1	TabletOral	OCEANSIDE PHARMACEUTICALS	68682-710
Enalapril Maleate	Enalapril maleate 5 mg/1	TabletOral	OCEANSIDE PHARMACEUTICALS	68682-711
Enalapril Maleate	Enalapril maleate 10 mg/1	TabletOral	OCEANSIDE PHARMACEUTICALS	68682-712
Enalapril Maleate	Enalapril maleate 20 mg/1	TabletOral	OCEANSIDE PHARMACEUTICALS	68682-713
Vasotecenalapril maleate	Enalapril maleate 2.5 mg/1	TabletOral	Bausch Health US LLC	0187-0140
Vasotecenalapril maleate	Enalapril maleate 5 mg/1	TabletOral	Bausch Health US LLC	0187-0141
Vasotecenalapril maleate	Enalapril maleate 10 mg/1	TabletOral	Bausch Health US LLC	0187-0142
Vasotecenalapril maleate	Enalapril maleate 20 mg/1	TabletOral	Bausch Health US LLC	0187-0143