NDC codes

FDA NDC Directory
Product NDC (as listed)66267-029Labeler and product segments. Claims need a package NDC.
Product NDC at billing width66267-0029Add 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
66267-029-30662670029306626700293030 TABLET in 1 BOTTLE (66267-029-30)Marketed from Sep 26, 2016
66267-029-60662670029606626700296060 TABLET in 1 BOTTLE (66267-029-60)Marketed from Sep 26, 2016
66267-029-90662670029906626700299090 TABLET in 1 BOTTLE (66267-029-90)Marketed from Sep 26, 2016

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 — 100 mg/1
Dosage form
Tablet
Route
Oral
Labeler
NuCare Pharmaceuticals, Inc.NDC labeler code 66267
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076900
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 66267-029_27353cec-1f04-8a8b-e063-6394a90af48eSPL ID 27353cec-1f04-8a8b-e063-6394a90af48eSPL set ID 3d70576a-6fa7-481d-e054-00144ff88e88RxCUI 197379UNII 50VV3VW0TIUPC 0366267029308
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

N466267002930 followed by a unit qualifier and the quantity

Package 66267-0029-30. 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)

INDICATIONS AND USAGE Hypertension Atenolol is 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 pressure g…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 66267-029

What is NDC 66267-029?
66267-029 is the product NDC for Atenolol, Atenolol 100 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals, Inc.. It has 3 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?
NuCare Pharmaceuticals, Inc., NDC labeler code 66267. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
AtenololAtenolol 50 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-92560760-0925-30
AtenololAtenolol 50 mg/1TabletOralCardinal Health 107, LLC55154-028355154-0283-00
AtenololAtenolol 100 mg/1TabletOralCoupler LLC67046-107667046-1076-03
AtenololAtenolol 25 mg/1TabletOralCoupler LLC67046-066367046-0663-03
AtenololAtenolol 50 mg/1TabletOralCoupler LLC67046-084367046-0843-03
AtenololAtenolol 100 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-411268788-4112-0168788-4112-0368788-4112-06+1 more
AtenololAtenolol 100 mg/1TabletOralSafecor Health, LLC48433-00648433-0006-20
AtenololAtenolol 25 mg/1TabletOralSafecor Health, LLC48433-00448433-0004-20
AtenololAtenolol 50 mg/1TabletOralSafecor Health, LLC48433-00548433-0005-20
AtenololAtenolol 50 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-883468788-8834-0168788-8834-0368788-8834-06+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
ProductStrengthForm · routeLabelerProduct NDC
AtenololAtenolol 25 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.43063-952
AtenololAtenolol 50 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-144
AtenololAtenolol 50 mg/1TabletOralA-S Medication Solutions50090-6779
AtenololAtenolol 50 mg/1TabletOralBryant Ranch Prepack71335-0912
AtenololAtenolol 25 mg/1TabletOralAmerican Health Packaging60687-605
AtenololAtenolol 25 mg/1TabletOralZydus Pharmaceuticals USA Inc.68382-022
AtenololAtenolol 50 mg/1TabletOralZydus Pharmaceuticals USA Inc.68382-023
AtenololAtenolol 100 mg/1TabletOralZydus Pharmaceuticals USA Inc.68382-024
AtenololAtenolol 50 mg/1TabletOralA-S Medication Solutions50090-0442
AtenololAtenolol 50 mg/1TabletOralZydus Lifesciences Limited65841-023
AtenololAtenolol 25 mg/1TabletOralZydus Lifesciences Limited65841-022
AtenololAtenolol 100 mg/1TabletOralZydus Lifesciences Limited65841-024

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