What is NDC 68788-4147?

68788-4147 is the product NDC for Enalapril Maleate, Enalapril maleate 20 mg/1 tablet, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.

Preferred Pharmaceuticals Inc., NDC labeler code 68788. 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 68788-4147 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68788-4147Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68788-4147Add 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
68788-4147-0	6878841470068788414700	100 TABLET in 1 BOTTLE (68788-4147-0)Marketed from Jul 10, 2026
68788-4147-3	6878841470368788414703	30 TABLET in 1 BOTTLE (68788-4147-3)Marketed from Jul 10, 2026
68788-4147-6	6878841470668788414706	60 TABLET in 1 BOTTLE (68788-4147-6)Marketed from Jul 10, 2026
68788-4147-9	6878841470968788414709	90 TABLET in 1 BOTTLE (68788-4147-9)Marketed from Jul 10, 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 — 20 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Preferred Pharmaceuticals Inc.NDC labeler code 68788
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 218531
Marketing start: Jul 10, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Angiotensin-converting Enzyme Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)
Identifiers: Product ID 68788-4147_eee8633b-9d9e-453d-8c6b-8b13c94d2f58SPL ID eee8633b-9d9e-453d-8c6b-8b13c94d2f58SPL set ID eee8633b-9d9e-453d-8c6b-8b13c94d2f58RxCUI 858810UNII 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

N468788414700 followed by a unit qualifier and the quantity

Package 68788-4147-00. 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 Jul 10, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Hypertension Enalapril maleate tablets, USP is indicated for the treatment of hypertension. Enalapril maleate tablets, USP is effective alone or in combination with other antihypertensive agents, especially thiazide-type diuretics. The blood pressure lowering effects of enalapril maleate and thiazides are approximately additive. Heart Failure Enalapril maleate tablets, USP is indicated for the treatment of symptomatic congestive heart failure, usually in combination with diuretics and digitalis. In these patients enalapril maleate improves symptoms, increases survival, and decreases the frequency of hospitalization (see for details and limitations of survival trials). A…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68788-4147

What is NDC 68788-4147?: 68788-4147 is the product NDC for Enalapril Maleate, Enalapril maleate 20 mg/1 tablet, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 4 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?: Preferred Pharmaceuticals Inc., NDC labeler code 68788. 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 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
Enalapril maleate	Enalapril maleate 10 mg/1	TabletOral	Major Pharmaceuticals	0904-7311	00904-7311-61

All 98 Enalapril Maleate NDCs

Other NDCs under ANDA 218531

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

FDA NDC Directory listings under ANDA 218531
Product	Strength	Form · route	Labeler	Product NDC
Enalapril Maleate	Enalapril maleate 5 mg/1	TabletOral	A-S Medication Solutions	50090-8131
Enalapril Maleate	Enalapril maleate 2.5 mg/1	TabletOral	Rising Pharma Holdings, Inc.	64980-685
Enalapril Maleate	Enalapril maleate 5 mg/1	TabletOral	Rising Pharma Holdings, Inc.	64980-686
Enalapril Maleate	Enalapril maleate 10 mg/1	TabletOral	Rising Pharma Holdings, Inc.	64980-687
Enalapril Maleate	Enalapril maleate 20 mg/1	TabletOral	Rising Pharma Holdings, Inc.	64980-688
Enalapril Maleate	Enalapril maleate 5 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4164
Enalapril Maleate	Enalapril maleate 10 mg/1	TabletOral	Bryant Ranch Prepack	71335-3136
Enalapril Maleate	Enalapril maleate 5 mg/1	TabletOral	Bryant Ranch Prepack	71335-3164