NDC codes

FDA NDC Directory
Product NDC (as listed)50090-5741Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-5741Add 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
50090-5741-05009057410050090574100100 TABLET in 1 BOTTLE (50090-5741-0)Marketed from Sep 29, 2021
50090-5741-1500905741015009057410130 TABLET in 1 BOTTLE (50090-5741-1)Marketed from Sep 29, 2021
50090-5741-4500905741045009057410460 TABLET in 1 BOTTLE (50090-5741-4)Marketed from Sep 29, 2021
50090-5741-75009057410750090574107200 TABLET in 1 BOTTLE (50090-5741-7)Marketed from Sep 29, 2021
50090-5741-8500905741085009057410890 TABLET in 1 BOTTLE (50090-5741-8)Marketed from Sep 29, 2021

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 — 50 mg/1
Dosage form
Tablet
Route
Oral
Labeler
A-S Medication SolutionsNDC labeler code 50090
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078512
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 50090-5741_2a2cb20e-d82d-4dab-8a26-4be38e8d02a2SPL ID 2a2cb20e-d82d-4dab-8a26-4be38e8d02a2SPL set ID 98471493-56ee-47a4-9120-0975c265361eRxCUI 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

N450090574100 followed by a unit qualifier and the quantity

Package 50090-5741-00. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

About NDC 50090-5741

What is NDC 50090-5741?
50090-5741 is the product NDC for Atenolol, Atenolol 50 mg/1 tablet, listed with the FDA by A-S Medication Solutions. 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?
A-S Medication Solutions, NDC labeler code 50090. 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 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
ProductStrengthForm · routeLabelerProduct NDC
AtenololAtenolol 50 mg/1TabletOralNorthwind Health Company, LLC51655-928
AtenololAtenolol 100 mg/1TabletOralBryant Ranch Prepack71335-2531
AtenololAtenolol 25 mg/1TabletOralAurobindo Pharma Limited65862-168
AtenololAtenolol 50 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3830
AtenololAtenolol 50 mg/1TabletOralAurobindo Pharma Limited65862-169
AtenololAtenolol 100 mg/1TabletOralAurobindo Pharma Limited65862-170
AtenololAtenolol 100 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3851
AtenololAtenolol 50 mg/1TabletOralREMEDYREPACK INC.70518-3036
AtenololAtenolol 25 mg/1TabletOralNorthwind Health Company, LLC51655-533
AtenololAtenolol 50 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8834
AtenololAtenolol 100 mg/1TabletOralNorthwind Health Company, LLC51655-104
AtenololAtenolol 25 mg/1TabletOralCoupler LLC67046-0663
AtenololAtenolol 100 mg/1TabletOralA-S Medication Solutions50090-5738
AtenololAtenolol 50 mg/1TabletOralQPharma Inc42708-162
AtenololAtenolol 50 mg/1TabletOralCoupler LLC67046-0843
AtenololAtenolol 25 mg/1TabletOralMajor Pharmaceuticals0904-7187
AtenololAtenolol 25 mg/1TabletOralREMEDYREPACK INC.70518-3531
AtenololAtenolol 100 mg/1TabletOralREMEDYREPACK INC.70518-4099
AtenololAtenolol 100 mg/1TabletOralCoupler LLC67046-1076
AtenololAtenolol 25 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-7876

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