Amlodipine Besylate and Benazepril Hydrochloride NDC 51655-201

NDC codes

FDA NDC Directory

Product NDC (as listed)51655-201Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51655-0201Add 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
51655-201-52	51655020152	30 CAPSULE in 1 BOTTLE, PLASTIC (51655-201-52)Marketed from Apr 19, 2023

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 Besylate and Benazepril Hydrochloride
Generic name (nonproprietary): amlodipine besylate and benazepril hydrochloride
Active ingredients: Benazepril hydrochloride — 20 mg/1Amlodipine besylate — 5 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Northwind Health Company, LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077183
Marketing start: Apr 19, 2023
Listing expires: Dec 31, 2027
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 51655-201_48c439c7-5726-89ae-e063-6394a90a41f6SPL ID 48c439c7-5726-89ae-e063-6394a90a41f6SPL set ID fa153720-b24c-60d0-e053-6294a90a97d5RxCUI 898356UNII N1SN99T69T, 864V2Q084H
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

N451655020152 followed by a unit qualifier and the quantity

Package 51655-0201-52. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 077183

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

FDA NDC Directory listings under ANDA 077183
Product	Strength	Form · route	Labeler	Product NDC
Amlodipine Besylate and Benazepril Hydrochloride	Amlodipine besylate 5 mg/1; Benazepril hydrochloride 10 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4499
Amlodipine Besylate and Benazepril Hydrochloride	Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1	CapsuleOral	Northwind Health Company, LLC	82868-041
Amlodipine Besylate and Benazepril Hydrochloride	Amlodipine besylate 5 mg/1; Benazepril hydrochloride 10 mg/1	CapsuleOral	Dr.Reddy's Laboratories Limited	55111-339
Amlodipine Besylate and Benazepril Hydrochloride	Amlodipine besylate 2.5 mg/1; Benazepril hydrochloride 10 mg/1	CapsuleOral	Dr.Reddy's Laboratories Limited	55111-338
Amlodipine Besylate and Benazepril Hydrochloride	Amlodipine besylate 5 mg/1; Benazepril hydrochloride 20 mg/1	CapsuleOral	Dr.Reddy's Laboratories Limited	55111-340
Amlodipine Besylate and Benazepril Hydrochloride	Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1	CapsuleOral	Dr.Reddy's Laboratories Limited	55111-341
Amlodipine Besylate and Benazepril Hydrochloride	Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1	CapsuleOral	A-S Medication Solutions	50090-5137