NDC codes

FDA NDC Directory
Product NDC (as listed)23155-923Labeler and product segments. Claims need a package NDC.
Product NDC at billing width23155-0923Add 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
23155-923-0123155092301100 CAPSULE in 1 BOTTLE (23155-923-01)Marketed from Jul 24, 2026
23155-923-0523155092305500 CAPSULE in 1 BOTTLE (23155-923-05)Marketed from Jul 24, 2026
23155-923-10231550923101000 CAPSULE in 1 BOTTLE (23155-923-10)Marketed from Jul 24, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
Amlodipine and Benazepril Hydrochloride
Generic name (nonproprietary)
amlodipine and benazepril hydrochloride
Active ingredients
Amlodipine besylate5 mg/1Benazepril hydrochloride40 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 091431
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 23155-923_ecbe2177-2319-4e49-a47a-48dd1aefe99fSPL ID ecbe2177-2319-4e49-a47a-48dd1aefe99fSPL set ID 27b0c628-820a-48bf-a411-86c0ebd4cc8dRxCUI 898342, 898346, 898350, 898353, 898356, 898359UNII 864V2Q084H, N1SN99T69TUPC 0323155923100, 0323155921052, 0323155924107, 0323155925012, 0323155920109, 0323155922059, 0323155924053, 0323155921014, 0323155924015, 0323155925104, 0323155920017, 0323155922103, 0323155921106, 0323155925050, 0323155920055, 0323155923018, 0323155923056, 0323155922011
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

N423155092301 followed by a unit qualifier and the quantity

Package 23155-0923-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Amlodipine and benazepril hydrochloride capsules are a combination capsule of amlodipine, a dihydropyridine calcium channel blocker (DHP CCB) and benazepril, an angiotensin-converting enzyme (ACE) inhibitor. Amlodipine and benazepril hydrochloride capsules are 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)

Other NDCs under ANDA 091431

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

FDA NDC Directory listings under ANDA 091431
ProductStrengthForm · routeLabelerProduct NDC
Amlodipine and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 40 mg/1CapsuleOralGolden State Medical Supply, Inc.84677-011
Amlodipine and Benazepril HydrochlorideAmlodipine besylate 2.5 mg/1; Benazepril hydrochloride 10 mg/1CapsuleOralGolden State Medical Supply, Inc.84677-008
Amlodipine and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 10 mg/1CapsuleOralGolden State Medical Supply, Inc.84677-009
Amlodipine and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 20 mg/1CapsuleOralGolden State Medical Supply, Inc.84677-010
Amlodipine and Benazepril HydrochlorideAmlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1CapsuleOralGolden State Medical Supply, Inc.84677-012
Amlodipine and Benazepril HydrochlorideAmlodipine besylate 10 mg/1; Benazepril hydrochloride 40 mg/1CapsuleOralGolden State Medical Supply, Inc.84677-013
Amlodipine and Benazepril HydrochlorideAmlodipine besylate 2.5 mg/1; Benazepril hydrochloride 10 mg/1CapsuleOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-920
Amlodipine and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 10 mg/1CapsuleOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-921
Amlodipine and Benazepril HydrochlorideAmlodipine besylate 5 mg/1; Benazepril hydrochloride 20 mg/1CapsuleOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-922
Amlodipine and Benazepril HydrochlorideAmlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1CapsuleOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-924
Amlodipine and Benazepril HydrochlorideAmlodipine besylate 10 mg/1; Benazepril hydrochloride 40 mg/1CapsuleOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-925

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