What is NDC 65841-022?

65841-022 is the product NDC for Atenolol, Atenolol 25 mg/1 tablet, 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 Atenolol?

124 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Atenolol NDC 65841-022 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)65841-022Labeler and product segments. Claims need a package NDC.

Product NDC at billing width65841-0022Add 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
65841-022-01	6584100220165841002201	100 TABLET in 1 BOTTLE (65841-022-01)Marketed from Oct 8, 2005
65841-022-10	6584100221065841002210	1000 TABLET in 1 BOTTLE (65841-022-10)Marketed from Oct 8, 2005
65841-022-16	6584100221665841002216	90 TABLET in 1 BOTTLE (65841-022-16)Marketed from Oct 8, 2005
65841-022-24	6584100222465841002224	10000 TABLET in 1 BOTTLE (65841-022-24)Marketed from Oct 8, 2005
65841-022-40	6584100224065841002240	5000 TABLET in 1 BOTTLE (65841-022-40)Marketed from Oct 8, 2005

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): Atenolol
Generic name (nonproprietary): atenolol
Active ingredients: Atenolol — 25 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Zydus Lifesciences LimitedNDC labeler code 65841
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076900
Marketing start: Oct 8, 2005
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 65841-022_f4fb6b85-6379-4e8a-9ee3-402819d128a0SPL ID f4fb6b85-6379-4e8a-9ee3-402819d128a0SPL set ID 2492d5f6-00b0-42c9-a793-2be83ea81ad1RxCUI 197379, 197380, 197381UNII 50VV3VW0TI
Pharmacologic class: beta-Adrenergic 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

N465841002201 followed by a unit qualifier and the quantity

Package 65841-0022-01. 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 Nov 25, 2024.

Full label on DailyMed (opens in a new tab)

About NDC 65841-022

What is NDC 65841-022?: 65841-022 is the product NDC for Atenolol, Atenolol 25 mg/1 tablet, 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?: Atenolol.
What is the active ingredient?: Atenolol.
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 Atenolol?: 124 other product NDCs are listed under this name. See all Atenolol 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 Atenolol NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Atenolol	Atenolol 50 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-925	60760-0925-30
Atenolol	Atenolol 50 mg/1	TabletOral	Cardinal Health 107, LLC	55154-0283	55154-0283-00
Atenolol	Atenolol 100 mg/1	TabletOral	Coupler LLC	67046-1076	67046-1076-03
Atenolol	Atenolol 25 mg/1	TabletOral	Coupler LLC	67046-0663	67046-0663-03
Atenolol	Atenolol 50 mg/1	TabletOral	Coupler LLC	67046-0843	67046-0843-03
Atenolol	Atenolol 100 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4112	68788-4112-0168788-4112-0368788-4112-06+1 more
Atenolol	Atenolol 100 mg/1	TabletOral	Safecor Health, LLC	48433-006	48433-0006-20
Atenolol	Atenolol 25 mg/1	TabletOral	Safecor Health, LLC	48433-004	48433-0004-20
Atenolol	Atenolol 50 mg/1	TabletOral	Safecor Health, LLC	48433-005	48433-0005-20
Atenolol	Atenolol 50 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8834	68788-8834-0168788-8834-0368788-8834-06+1 more

All 125 Atenolol NDCs

Other NDCs under ANDA 076900

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

FDA NDC Directory listings under ANDA 076900
Product	Strength	Form · route	Labeler	Product NDC
Atenolol	Atenolol 25 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-952
Atenolol	Atenolol 50 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-144
Atenolol	Atenolol 50 mg/1	TabletOral	A-S Medication Solutions	50090-6779
Atenolol	Atenolol 50 mg/1	TabletOral	Bryant Ranch Prepack	71335-0912
Atenolol	Atenolol 25 mg/1	TabletOral	American Health Packaging	60687-605
Atenolol	Atenolol 25 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	68382-022
Atenolol	Atenolol 50 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	68382-023
Atenolol	Atenolol 100 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	68382-024
Atenolol	Atenolol 50 mg/1	TabletOral	A-S Medication Solutions	50090-0442
Atenolol	Atenolol 50 mg/1	TabletOral	Zydus Lifesciences Limited	65841-023
Atenolol	Atenolol 100 mg/1	TabletOral	Zydus Lifesciences Limited	65841-024
Atenolol	Atenolol 100 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	66267-029