NDC codes

FDA NDC Directory
Product NDC (as listed)68071-4751Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-4751Add 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
68071-4751-96807147510990 TABLET in 1 BOTTLE (68071-4751-9)Marketed from Feb 6, 2025

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
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077443
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 68071-4751_2d7cebf6-1450-8db6-e063-6394a90ace85SPL ID 2d7cebf6-1450-8db6-e063-6394a90ace85SPL set ID 8115a2bc-69aa-60b4-e053-2a91aa0aeae7RxCUI 197379UNII 50VV3VW0TIUPC 0368071475197
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

N468071475109 followed by a unit qualifier and the quantity

Package 68071-4751-09. 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.

Other NDCs under ANDA 077443

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

FDA NDC Directory listings under ANDA 077443
ProductStrengthForm · routeLabelerProduct NDC
AtenololAtenolol 25 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4538
AtenololAtenolol 25 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8527
AtenololAtenolol 25 mg/1TabletOralDirect_Rx72189-396
AtenololAtenolol 50 mg/1TabletOralBryant Ranch Prepack71335-0954
AtenololAtenolol 50 mg/1TabletOralA-S Medication Solutions50090-5367
AtenololAtenolol 50 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4527
AtenololAtenolol 50 mg/1TabletOraldirect rx72189-135
AtenololAtenolol 100 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-5162
atenololAtenolol 100 mg/1TabletOraldirect rx72189-152
AtenololAtenolol 25 mg/1TabletOralProficient Rx LP71205-096
AtenololAtenolol 100 mg/1TabletOralPreferred Pharmaceuticals, Inc.68788-7535
AtenololAtenolol 25 mg/1TabletOralBryant Ranch Prepack71335-1535
AtenololAtenolol 25 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8372
AtenololAtenolol 50 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8373
AtenololAtenolol 25 mg/1TabletOralNorthwind Health Company, LLC51655-709
AtenololAtenolol 50 mg/1TabletOralPreferred Pharmaceuticals, Inc.68788-7616
AtenololAtenolol 50 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4553
AtenololAtenolol 50 mg/1TabletOralProficient Rx LP71205-229
AtenololAtenolol 25 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-437
AtenololAtenolol 100 mg/1TabletOralBryant Ranch Prepack71335-1264

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