NDC codes

FDA NDC Directory
Product NDC (as listed)43063-765Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43063-0765Add 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
43063-765-30430630765304306307653030 TABLET in 1 BOTTLE, PLASTIC (43063-765-30)Marketed from May 11, 2017
43063-765-90430630765904306307659090 TABLET in 1 BOTTLE, PLASTIC (43063-765-90)Marketed from Dec 18, 2017

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 — 50 mg/1
Dosage form
Tablet
Route
Oral
Labeler
PD-Rx Pharmaceuticals, Inc.NDC labeler code 43063
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 074056
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 43063-765_414b8e3f-9bc8-52f4-e063-6294a90a0eb3SPL ID 414b8e3f-9bc8-52f4-e063-6294a90a0eb3SPL set ID c69b8e5e-c7c3-4883-9cea-f7f435a8ede8RxCUI 197381UNII 50VV3VW0TIUPC 0343063765906
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

N443063076530 followed by a unit qualifier and the quantity

Package 43063-0765-30. 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 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 43063-765

What is NDC 43063-765?
43063-765 is the product NDC for Atenolol, Atenolol 50 mg/1 tablet, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 2 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?
PD-Rx Pharmaceuticals, Inc., NDC labeler code 43063. 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 074056

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

FDA NDC Directory listings under ANDA 074056
ProductStrengthForm · routeLabelerProduct NDC
AtenololAtenolol 50 mg/1TabletOralTeva Pharmaceuticals USA, Inc.0093-0752
AtenololAtenolol 100 mg/1TabletOralTeva Pharmaceuticals USA, Inc.0093-0753
AtenololAtenolol 25 mg/1TabletOralTeva Pharmaceuticals USA, Inc.0093-0787
AtenololAtenolol 50 mg/1TabletOralQPharma, Inc.42708-012
AtenololAtenolol 25 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.43063-805
AtenololAtenolol 25 mg/1TabletOralA-S Medication Solutions50090-3411
AtenololAtenolol 25 mg/1TabletOralA-S Medication Solutions50090-6935
AtenololAtenolol 25 mg/1TabletOralProficient Rx LP63187-537
AtenololAtenolol 50 mg/1TabletOralProficient Rx LP63187-710
AtenololAtenolol 25 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4526
AtenololAtenolol 25 mg/1TabletOralBryant Ranch Prepack71335-1616
AtenololAtenolol 25 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-857
AtenololAtenolol 50 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-861

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