What is NDC 68071-3694?

68071-3694 is the product NDC for Atenolol 29300-411 (atenolol), Atenolol 50 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

NuCare Pharmaceuticals,Inc., NDC labeler code 68071. 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 29300-411?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Atenolol 29300-411 NDC 68071-3694 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68071-3694Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68071-3694Add 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 NDC	11-digit (billing)	Package	Copy
68071-3694-1	6807136940168071369401	100 TABLET in 1 BOTTLE (68071-3694-1)Marketed from Oct 3, 2024

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 29300-411Suffix: 29300-411
Generic name (nonproprietary): atenolol
Active ingredients: Atenolol — 50 mg/1
Dosage form: Tablet
Route: Oral
Labeler: NuCare Pharmaceuticals,Inc.NDC labeler code 68071
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213136
Marketing start: Nov 21, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 68071-3694_2a31d713-770d-8310-e063-6394a90a2406SPL ID 2a31d713-770d-8310-e063-6394a90a2406SPL set ID 239b1cce-3b1a-f049-e063-6394a90a0e0aRxCUI 197381UNII 50VV3VW0TIUPC 0368071369410
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

N468071369401 followed by a unit qualifier and the quantity

Package 68071-3694-01. 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 Dec 26, 2024.

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 68071-3694

What is NDC 68071-3694?: 68071-3694 is the product NDC for Atenolol 29300-411 (atenolol), Atenolol 50 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Atenolol 29300-411 (Atenolol).
What is the active ingredient?: Atenolol.
Who is the labeler?: NuCare Pharmaceuticals,Inc., NDC labeler code 68071. 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 29300-411?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under ANDA 213136

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

FDA NDC Directory listings under ANDA 213136
Product	Strength	Form · route	Labeler	Product NDC
Atenolol	Atenolol 25 mg/1	TabletOral	Unichem Pharmaceuticals (USA), Inc.	29300-410
Atenolol	Atenolol 50 mg/1	TabletOral	Unichem Pharmaceuticals (USA), Inc.	29300-411
Atenolol	Atenolol 100 mg/1	TabletOral	Unichem Pharmaceuticals (USA), Inc.	29300-412
Atenolol	Atenolol 50 mg/1	TabletOral	A-S Medication Solutions	50090-5363
Atenolol	Atenolol 25 mg/1	TabletOral	A-S Medication Solutions	50090-6241
Atenolol	Atenolol 100 mg/1	TabletOral	A-S Medication Solutions	50090-6311
Atenolol	Atenolol 50 mg/1	TabletOral	A-S Medication Solutions	50090-7561
Atenolol	Atenolol 25 mg/1	TabletOral	A-S Medication Solutions	50090-7603
Atenolol	Atenolol 50 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-925
Atenolol	Atenolol 100 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4112
Atenolol	Atenolol 25 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8739
Atenolol	Atenolol 25 mg/1	TabletOral	REMEDYREPACK INC.	70518-4287
Atenolol	Atenolol 100 mg/1	TabletOral	Bryant Ranch Prepack	71335-2774
Atenolol	Atenolol 25 mg/1	TabletOral	Bryant Ranch Prepack	71335-9611
Atenolol	Atenolol 50 mg/1	TabletOral	Quality Care Products, LLC	83008-052
Atenolol	Atenolol 25 mg/1	TabletOral	ASCLEMED USA INC.	87063-177
Atenolol	Atenolol 50 mg/1	TabletOral	ASCLEMED USA INC.	87063-178
Atenolol	Atenolol 100 mg/1	TabletOral	ASCLEMED USA INC.	87063-179

Atenolol 29300-411 (Atenolol) NDC 68071-3694