What is NDC 65841-656?

65841-656 is the product NDC for Ramipril, Ramipril 2.5 mg/1 capsule, listed with the FDA by Zydus Lifesciences Limited. It has 5 package NDCs, shown above in 10- and 11-digit form.

Zydus Lifesciences Limited, NDC labeler code 65841. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Ramipril?

68 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Ramipril NDC 65841-656 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)65841-656Labeler and product segments. Claims need a package NDC.

Product NDC at billing width65841-0656Add 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
65841-656-01	6584106560165841065601	100 CAPSULE in 1 BOTTLE (65841-656-01)Marketed from Nov 20, 2010
65841-656-05	6584106560565841065605	500 CAPSULE in 1 BOTTLE (65841-656-05)Marketed from Nov 20, 2010
65841-656-06	6584106560665841065606	30 CAPSULE in 1 BOTTLE (65841-656-06)Marketed from Nov 20, 2010
65841-656-16	6584106561665841065616	90 CAPSULE in 1 BOTTLE (65841-656-16)Marketed from Nov 20, 2010
65841-656-30	6584106563065841065630	10 BLISTER PACK in 1 CARTON (65841-656-30) / 10 CAPSULE in 1 BLISTER PACKMarketed from Nov 20, 2010

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): Ramipril
Generic name (nonproprietary): ramipril
Active ingredients: Ramipril — 2.5 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Zydus Lifesciences LimitedNDC labeler code 65841
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078832
Marketing start: Nov 20, 2010
Listing expires: Dec 31, 2027
Other FDA classes: Angiotensin-converting Enzyme Inhibitors (Mechanism)
Identifiers: Product ID 65841-656_1d7227b2-6052-40b4-bf22-29f18672ce08SPL ID 1d7227b2-6052-40b4-bf22-29f18672ce08SPL set ID 496b346b-ca79-4483-a950-bed9464e6a9dRxCUI 198188, 198189, 261962, 845488UNII L35JN3I7SJ
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

N465841065601 followed by a unit qualifier and the quantity

Package 65841-0656-01. 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 Dec 4, 2024.

Full label on DailyMed (opens in a new tab)

About NDC 65841-656

What is NDC 65841-656?: 65841-656 is the product NDC for Ramipril, Ramipril 2.5 mg/1 capsule, listed with the FDA by Zydus Lifesciences Limited. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Ramipril.
What is the active ingredient?: Ramipril.
Who is the labeler?: Zydus Lifesciences Limited, NDC labeler code 65841. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ramipril?: 68 other product NDCs are listed under this name. See all Ramipril 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 Ramipril NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Ramipril	Ramipril 2.5 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4604	70518-4604-00
Ramipril	Ramipril 5 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4607	70518-4607-00
Ramipril	Ramipril 2.5 mg/1	CapsuleOral	GSMS, Incorporated	51407-707	51407-0707-01
Ramipril	Ramipril 5 mg/1	CapsuleOral	GSMS, Incorporated	51407-708	51407-0708-01
Ramipril	Ramipril 10 mg/1	CapsuleOral	GSMS, Incorporated	51407-709	51407-0709-01
Ramipril	Ramipril 10 mg/1	CapsuleOral	Northwind Health Company, LLC	51655-904	51655-0904-2651655-0904-52
Ramipril	Ramipril 2.5 mg/1	CapsuleOral	Northwind Health Company, LLC	51655-975	51655-0975-52
Ramipril	Ramipril 5 mg/1	CapsuleOral	Northwind Health Company, LLC	51655-296	51655-0296-52
Ramipril	Ramipril 10 mg/1	CapsuleOral	Northwind Health Company, LLC	51655-406	51655-0406-52
Ramipril	Ramipril 10 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-3038	70518-3038-00

All 69 Ramipril NDCs

Other NDCs under ANDA 078832

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

FDA NDC Directory listings under ANDA 078832
Product	Strength	Form · route	Labeler	Product NDC
Ramipril	Ramipril 1.25 mg/1	CapsuleOral	Zydus Lifesciences Limited	65841-655
Ramipril	Ramipril 5 mg/1	CapsuleOral	Zydus Lifesciences Limited	65841-657
Ramipril	Ramipril 10 mg/1	CapsuleOral	Zydus Lifesciences Limited	65841-658
Ramipril	Ramipril 1.25 mg/1	CapsuleOral	Zydus Pharmaceuticals USA Inc.	68382-144
Ramipril	Ramipril 2.5 mg/1	CapsuleOral	Zydus Pharmaceuticals USA Inc.	68382-145
Ramipril	Ramipril 5 mg/1	CapsuleOral	Zydus Pharmaceuticals USA Inc.	68382-146
Ramipril	Ramipril 10 mg/1	CapsuleOral	Zydus Pharmaceuticals USA Inc.	68382-147
Ramipril	Ramipril 2.5 mg/1	CapsuleOral	PD-Rx Pharmaceuticals, Inc.	72789-415