What is NDC 71335-3085?

71335-3085 is the product NDC for Enalapril Maleate, Enalapril maleate 2.5 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 2 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. 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 71335-3085 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-3085Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-3085Add 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	Copy
71335-3085-1	7133530850171335308501	30 TABLET in 1 BOTTLE (71335-3085-1)Marketed from Feb 16, 2026
71335-3085-2	7133530850271335308502	90 TABLET in 1 BOTTLE (71335-3085-2)Marketed from Feb 16, 2026

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 — 2.5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213273
Marketing start: Jul 31, 2022
Listing expires: Dec 31, 2027
Other FDA classes: Angiotensin-converting Enzyme Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)
Identifiers: Product ID 71335-3085_7eb9137b-860a-40a3-be6c-20e32164a9fcSPL ID 7eb9137b-860a-40a3-be6c-20e32164a9fcSPL set ID 2a8ca159-c4c7-468a-bcc2-d1b879ea2c7eRxCUI 858804UNII 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

N471335308501 followed by a unit qualifier and the quantity

Package 71335-3085-01. 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 Feb 16, 2026. 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 thiazidetype 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, increase survival, and decrease the frequency of hospitalization (see CLINICAL PHARMACOLOGY, Heart Failure, Mortality Tr…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-3085

What is NDC 71335-3085?: 71335-3085 is the product NDC for Enalapril Maleate, Enalapril maleate 2.5 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 2 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?: Bryant Ranch Prepack, NDC labeler code 71335. 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 ANDA 213273

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

FDA NDC Directory listings under ANDA 213273
Product	Strength	Form · route	Labeler	Product NDC
Enalapril Maleate	Enalapril maleate 2.5 mg/1	TabletOral	Solco Healthcare US, LLC	43547-545
Enalapril Maleate	Enalapril maleate 5 mg/1	TabletOral	Solco Healthcare US, LLC	43547-546
Enalapril Maleate	Enalapril maleate 10 mg/1	TabletOral	Solco Healthcare US, LLC	43547-547
Enalapril Maleate	Enalapril maleate 20 mg/1	TabletOral	Solco Healthcare US, LLC	43547-548
Enalapril Maleate	Enalapril maleate 5 mg/1	TabletOral	A-S Medication Solutions	50090-7302
Enalapril Maleate	Enalapril maleate 20 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-575
Enalapril Maleate	Enalapril maleate 10 mg/1	TabletOral	Coupler LLC	67046-0798
Enalapril Maleate	Enalapril maleate 2.5 mg/1	TabletOral	Coupler LLC	67046-1254
Enalapril Maleate	Enalapril maleate 5 mg/1	TabletOral	Coupler LLC	67046-1504
Enalapril Maleate	Enalapril maleate 10 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-1793
Enalapril Maleate	Enalapril maleate 20 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3408
Enalapril Maleate	Enalapril maleate 10 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3537
Enalapril Maleate	Enalapril maleate 20 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-3820
Enalapril Maleate	Enalapril maleate 20 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8320
Enalapril Maleate	Enalapril maleate 10 mg/1	TabletOral	Preferred Pharmaceuicals Inc.	68788-8385
Enalapril Maleate	Enalapril maleate 5 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8437
Enalapril Maleate	Enalapril maleate 5 mg/1	TabletOral	REMEDYREPACK INC.	70518-3572
Enalapril Maleate	Enalapril maleate 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-4011
Enalapril Maleate	Enalapril maleate 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-4197
Enalapril Maleate	Enalapril maleate 2.5 mg/1	TabletOral	REMEDYREPACK INC.	70518-4210

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