What is NDC 71335-2531?

71335-2531 is the product NDC for Atenolol, Atenolol 100 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 7 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. 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 71335-2531 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-2531Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-2531Add 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
71335-2531-1	7133525310171335253101	100 TABLET in 1 BOTTLE (71335-2531-1)Marketed from Nov 26, 2024
71335-2531-2	7133525310271335253102	30 TABLET in 1 BOTTLE (71335-2531-2)Marketed from Nov 26, 2024
71335-2531-3	7133525310371335253103	60 TABLET in 1 BOTTLE (71335-2531-3)Marketed from Nov 26, 2024
71335-2531-4	7133525310471335253104	90 TABLET in 1 BOTTLE (71335-2531-4)Marketed from Nov 26, 2024
71335-2531-5	7133525310571335253105	20 TABLET in 1 BOTTLE (71335-2531-5)Marketed from Nov 26, 2024
71335-2531-6	7133525310671335253106	180 TABLET in 1 BOTTLE (71335-2531-6)Marketed from Nov 26, 2024
71335-2531-7	7133525310771335253107	10 TABLET in 1 BOTTLE (71335-2531-7)Marketed from Nov 26, 2024

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

Brand name (proprietary): Atenolol
Generic name (nonproprietary): atenolol
Active ingredients: Atenolol — 100 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078512
Marketing start: Oct 31, 2007
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 71335-2531_e2d819f9-b7db-4c40-9ce9-953d58aa371cSPL ID e2d819f9-b7db-4c40-9ce9-953d58aa371cSPL set ID 09b21985-1818-449d-9b29-98f733cf7b9fRxCUI 197379UNII 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

N471335253101 followed by a unit qualifier and the quantity

Package 71335-2531-01. 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 26, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Hypertension Atenolol tablets are indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure lowers the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including atenolol. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will require more than 1 drug to achieve blood p…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-2531

What is NDC 71335-2531?: 71335-2531 is the product NDC for Atenolol, Atenolol 100 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 7 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?: Bryant Ranch Prepack, NDC labeler code 71335. 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 078512

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

FDA NDC Directory listings under ANDA 078512
Product	Strength	Form · route	Labeler	Product NDC
Atenolol	Atenolol 50 mg/1	TabletOral	Northwind Health Company, LLC	51655-928
Atenolol	Atenolol 25 mg/1	TabletOral	Aurobindo Pharma Limited	65862-168
Atenolol	Atenolol 50 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3830
Atenolol	Atenolol 50 mg/1	TabletOral	Aurobindo Pharma Limited	65862-169
Atenolol	Atenolol 100 mg/1	TabletOral	Aurobindo Pharma Limited	65862-170
Atenolol	Atenolol 100 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3851
Atenolol	Atenolol 50 mg/1	TabletOral	REMEDYREPACK INC.	70518-3036
Atenolol	Atenolol 25 mg/1	TabletOral	Northwind Health Company, LLC	51655-533
Atenolol	Atenolol 50 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8834
Atenolol	Atenolol 100 mg/1	TabletOral	Northwind Health Company, LLC	51655-104
Atenolol	Atenolol 25 mg/1	TabletOral	Coupler LLC	67046-0663
Atenolol	Atenolol 100 mg/1	TabletOral	A-S Medication Solutions	50090-5738
Atenolol	Atenolol 50 mg/1	TabletOral	A-S Medication Solutions	50090-5741
Atenolol	Atenolol 50 mg/1	TabletOral	QPharma Inc	42708-162
Atenolol	Atenolol 50 mg/1	TabletOral	Coupler LLC	67046-0843
Atenolol	Atenolol 25 mg/1	TabletOral	Major Pharmaceuticals	0904-7187
Atenolol	Atenolol 25 mg/1	TabletOral	REMEDYREPACK INC.	70518-3531
Atenolol	Atenolol 100 mg/1	TabletOral	REMEDYREPACK INC.	70518-4099
Atenolol	Atenolol 100 mg/1	TabletOral	Coupler LLC	67046-1076
Atenolol	Atenolol 25 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-7876