What is NDC 63629-7895?

63629-7895 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 63629. 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 63629-7895 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)63629-7895Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63629-7895Add 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
63629-7895-1	6362978950163629789501	30 TABLET in 1 BOTTLE (63629-7895-1)Marketed from Jan 15, 2019
63629-7895-2	6362978950263629789502	90 TABLET in 1 BOTTLE (63629-7895-2)Marketed from Jan 15, 2019

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 63629
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 075657
Marketing start: Jan 23, 2001
Listing expires: Dec 31, 2027
Other FDA classes: Angiotensin-converting Enzyme Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)
Identifiers: Product ID 63629-7895_b64a2a17-b933-48eb-9a54-02a701dcefe9SPL ID b64a2a17-b933-48eb-9a54-02a701dcefe9SPL set ID fb3c7066-76cb-4e8e-b98b-bcb41a3631dfRxCUI 858804, 858810, 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

N463629789501 followed by a unit qualifier and the quantity

Package 63629-7895-01. 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 Aug 11, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Hypertension Enalapril maleate is indicated for the treatment of hypertension. Enalapril maleate 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 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 CLINICAL PHARMACOLOGY, Heart Failure, Mortality Trials for details and limitations of sur…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63629-7895

What is NDC 63629-7895?: 63629-7895 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 63629. 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 075657

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

FDA NDC Directory listings under ANDA 075657
Product	Strength	Form · route	Labeler	Product NDC
Enalapril Maleate	Enalapril maleate 5 mg/1	TabletOral	Bryant Ranch Prepack	71335-1910
Enalapril Maleate	Enalapril maleate 5 mg/1	TabletOral	Sun Pharmaceutical Industries, Inc.	51672-4038
Enalapril Maleate	Enalapril maleate 2.5 mg/1	TabletOral	Sun Pharmaceutical Industries, Inc.	51672-4037
Enalapril Maleate	Enalapril maleate 20 mg/1	TabletOral	Sun Pharmaceutical Industries, Inc.	51672-4040
Enalapril Maleate	Enalapril maleate 10 mg/1	TabletOral	Golden State Medical Supply, Inc.	51407-828
Enalapril Maleate	Enalapril maleate 20 mg/1	TabletOral	Northwind Health Company, LLC	51655-341
Enalapril Maleate	Enalapril maleate 20 mg/1	TabletOral	Bryant Ranch Prepack	71335-9649
Enalapril Maleate	Enalapril maleate 10 mg/1	TabletOral	A-S Medication Solutions	50090-6712
Enalapril Maleate	Enalapril maleate 2.5 mg/1	TabletOral	Bryant Ranch Prepack	71335-2252
Enalapril Maleate	Enalapril maleate 10 mg/1	TabletOral	Sun Pharmaceutical Industries, Inc.	51672-4245
Enalapril Maleate	Enalapril maleate 20 mg/1	TabletOral	A-S Medication Solutions	50090-4560
Enalapril Maleate	Enalapril maleate 20 mg/1	TabletOral	Proficient Rx LP	63187-977
Enalapril Maleate	Enalapril maleate 5 mg/1	TabletOral	A-S Medication Solutions	50090-3378
Enalapril Maleate	Enalapril maleate 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-4256
Enalapril Maleate	Enalapril maleate 10 mg/1	TabletOral	Bryant Ranch Prepack	71335-2608
Enalapril Maleate	Enalapril maleate 20 mg/1	TabletOral	Golden State Medical Supply, Inc.	60429-186
Enalapril Maleate	Enalapril maleate 2.5 mg/1	TabletOral	Golden State Medical Supply, Inc.	60429-183
Enalapril Maleate	Enalapril maleate 5 mg/1	TabletOral	Golden State Medical Supply, Inc.	60429-184