What is NDC 70518-4197?

70518-4197 is the product NDC for Enalapril Maleate, Enalapril maleate 10 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 3 package NDCs, shown above in 10- and 11-digit form.

REMEDYREPACK INC., NDC labeler code 70518. 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 70518-4197 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-4197Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-4197Add 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
70518-4197-0	7051841970070518419700	90 TABLET in 1 BOTTLE, PLASTIC (70518-4197-0)Marketed from Oct 1, 2024
70518-4197-1	7051841970170518419701	30 TABLET in 1 BLISTER PACK (70518-4197-1)Marketed from May 3, 2025
70518-4197-2	7051841970270518419702	90 TABLET in 1 BOTTLE, PLASTIC (70518-4197-2)Marketed from Jul 13, 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 — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: REMEDYREPACK INC.NDC labeler code 70518
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213273
Marketing start: Oct 1, 2024
Listing expires: Dec 31, 2027
Other FDA classes: Angiotensin-converting Enzyme Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)
Identifiers: Product ID 70518-4197_5a57ebd9-07fe-cfdf-e063-6294a90a98cbSPL ID 5a57ebd9-07fe-cfdf-e063-6294a90a98cbSPL set ID 5118eb9f-1466-4318-b17e-cf5898edbeefRxCUI 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

N470518419700 followed by a unit qualifier and the quantity

Package 70518-4197-00. 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 Aug 31, 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 70518-4197

What is NDC 70518-4197?: 70518-4197 is the product NDC for Enalapril Maleate, Enalapril maleate 10 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. 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?: REMEDYREPACK INC., NDC labeler code 70518. 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 2.5 mg/1	TabletOral	REMEDYREPACK INC.	70518-4210
Enalapril Maleate	Enalapril maleate 5 mg/1	TabletOral	Bryant Ranch Prepack	71335-2382

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