NDC codes

FDA NDC Directory
Product NDC (as listed)50090-3411Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-3411Add 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
50090-3411-05009034110030 TABLET in 1 BOTTLE, PLASTIC (50090-3411-0)Marketed from Nov 28, 2014
50090-3411-250090341102100 TABLET in 1 BOTTLE, PLASTIC (50090-3411-2)Marketed from Nov 28, 2014
50090-3411-55009034110590 TABLET in 1 BOTTLE (50090-3411-5)Marketed from Mar 22, 2018

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 — 25 mg/1
Dosage form
Tablet
Route
Oral
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 50090-3411_2d5678ea-4f8e-4271-a7f3-cf9f9c2cee9cSPL ID 2d5678ea-4f8e-4271-a7f3-cf9f9c2cee9c
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

N450090341100 followed by a unit qualifier and the quantity

Package 50090-3411-00. 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

The FDA listing for this product does not reference a label (SPL) set.

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 25 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4526
AtenololAtenolol 50 mg/1TabletOralProficient Rx LP63187-710
AtenololAtenolol 25 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-857
AtenololAtenolol 50 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-861
AtenololAtenolol 50 mg/1TabletOralTeva Pharmaceuticals USA, Inc.0093-0752
AtenololAtenolol 100 mg/1TabletOralTeva Pharmaceuticals USA, Inc.0093-0753
AtenololAtenolol 25 mg/1TabletOralBryant Ranch Prepack71335-1616
AtenololAtenolol 50 mg/1TabletOralQPharma, Inc.42708-012
AtenololAtenolol 25 mg/1TabletOralTeva Pharmaceuticals USA, Inc.0093-0787
AtenololAtenolol 25 mg/1TabletOralA-S Medication Solutions50090-6935
AtenololAtenolol 25 mg/1TabletOralProficient Rx LP63187-537
AtenololAtenolol 50 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.43063-765
AtenololAtenolol 25 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.43063-805

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Atenolol NDC 50090-3411 | Med-Code