NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4382Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4382Add 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 NDC11-digit (billing)PackageCopy
70518-4382-0705184382007051843820090 CAPSULE in 1 BOTTLE, PLASTIC (70518-4382-0)Marketed from Jul 2, 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

Generic name (nonproprietary)
amlodipine besylate and benazepril hydrochloride
Active ingredients
Amlodipine besylate — 10 mg/1Benazepril hydrochloride — 40 mg/1
Dosage form
Capsule
Route
Oral
Labeler
REMEDYREPACK INC.NDC labeler code 70518
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078466
Marketing start
Listing expires
Other FDA classes
Angiotensin-converting Enzyme Inhibitors (Mechanism)Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)Dihydropyridines (Chemical structure)
Identifiers
Product ID 70518-4382_5b0f427c-1c73-81b4-e063-6294a90adaebSPL ID 5b0f427c-1c73-81b4-e063-6294a90adaebSPL set ID 0f253cac-67ac-4b03-b1a8-f2c345938ddaRxCUI 898346UNII 864V2Q084H, N1SN99T69T
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker

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

N470518438200 followed by a unit qualifier and the quantity

Package 70518-4382-00. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Amlodipine and benazepril hydrochloride capsule, is a combination capsule of amlodipine, a dihydropyridine calcium channel blocker (DHP CCB) and benazepril, an angiotensin converting-enzyme (ACE) inhibitor. Amlodipine and benazepril hydrochloride capsule, is indicated for the treatment of hypertension in patients not adequately controlled on monotherapy with either agent ( 1 ). 1.1 Hypertension Amlodipine and benazepril hydrochloride capsules are indicated for the treatment of hypertension in patients not adequately controlled on monotherapy with either agent.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70518-4382

What is NDC 70518-4382?
70518-4382 is the product NDC for Amlodipine Besylate and Benazepril Hydrochloride, Amlodipine besylate 10 mg/1; Benazepril hydrochloride 40 mg/1 capsule, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Amlodipine Besylate and Benazepril Hydrochloride.
What is the active ingredient?
Amlodipine besylate, Benazepril hydrochloride.
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 Amlodipine Besylate and Benazepril Hydrochloride?
47 other product NDCs are listed under this name. See all Amlodipine Besylate and Benazepril Hydrochloride 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 Amlodipine Besylate and Benazepril Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 2.5 mg/1; Benazepril hydrochloride 10 mg/1CapsuleOralAmneal Pharmaceuticals NY LLC69238-268469238-2684-01
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 10 mg/1CapsuleOralAmneal Pharmaceuticals NY LLC69238-268569238-2685-01
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 20 mg/1CapsuleOralAmneal Pharmaceuticals NY LLC69238-268669238-2686-01
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1CapsuleOralAmneal Pharmaceuticals NY LLC69238-268769238-2687-01
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 10 mg/1CapsuleOralREMEDYREPACK INC.70518-449970518-4499-00
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 20 mg/1CapsuleOralREMEDYREPACK INC.70518-438670518-4386-00
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 40 mg/1CapsuleOralREMEDYREPACK INC.70518-438870518-4388-00
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-881868788-8818-03
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1CapsuleOralNorthwind Health Company, LLC82868-04182868-0041-90
Amlodipine Besylate and Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1; Amlodipine besylate 5 mg/1CapsuleOralNorthwind Health Company, LLC51655-20151655-0201-52

All 48 Amlodipine Besylate and Benazepril Hydrochloride NDCs

Other NDCs under ANDA 078466

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

FDA NDC Directory listings under ANDA 078466
ProductStrengthForm · routeLabelerProduct NDC
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 40 mg/1CapsuleOralA-S Medication Solutions50090-5357
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 10 mg/1; Benazepril hydrochloride 40 mg/1CapsuleOralA-S Medication Solutions50090-5389
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 10 mg/1CapsuleOralA-S Medication Solutions50090-5404
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 20 mg/1CapsuleOralA-S Medication Solutions50090-6185
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1CapsuleOralA-S Medication Solutions50090-6427
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1CapsuleOralBluePoint Laboratories68001-130
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 10 mg/1; Benazepril hydrochloride 40 mg/1CapsuleOralBluePoint Laboratories68001-131
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 2.5 mg/1; Benazepril hydrochloride 10 mg/1CapsuleOralBluePoint Laboratories68001-132
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 10 mg/1CapsuleOralBluePoint Laboratories68001-133
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 20 mg/1CapsuleOralBluePoint Laboratories68001-134
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 40 mg/1CapsuleOralBluePoint Laboratories68001-135
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 20 mg/1CapsuleOralLupin Pharmaceuticals, Inc.68180-459
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 40 mg/1CapsuleOralLupin Pharmaceuticals, Inc.68180-463
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1CapsuleOralLupin Pharmaceuticals, Inc.68180-472
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 10 mg/1; Benazepril hydrochloride 40 mg/1CapsuleOralLupin Pharmaceuticals, Inc.68180-473
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 2.5 mg/1; Benazepril hydrochloride 10 mg/1CapsuleOralLupin Pharmaceuticals, Inc.68180-755
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 10 mg/1CapsuleOralLupin Pharmaceuticals, Inc.68180-756
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 20 mg/1CapsuleOralLupin Pharmaceuticals, Inc.68180-757
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1CapsuleOralLupin Pharmaceuticals, Inc.68180-758
Amlodipine Besylate and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 40 mg/1CapsuleOralLupin Pharmaceuticals, Inc.68180-759

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