What is NDC 71335-3178?

71335-3178 is the product NDC for Atenolol, Atenolol 100 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 7 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. 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?

123 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Atenolol NDC 71335-3178 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-3178Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-3178Add 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
71335-3178-1	71335317801	100 TABLET in 1 BOTTLE (71335-3178-1)Marketed from Sep 24, 2026
71335-3178-2	71335317802	30 TABLET in 1 BOTTLE (71335-3178-2)Marketed from Sep 24, 2026
71335-3178-3	71335317803	60 TABLET in 1 BOTTLE (71335-3178-3)Marketed from Sep 24, 2026
71335-3178-4	71335317804	90 TABLET in 1 BOTTLE (71335-3178-4)Marketed from Sep 24, 2026
71335-3178-5	71335317805	20 TABLET in 1 BOTTLE (71335-3178-5)Marketed from Sep 24, 2026
71335-3178-6	71335317806	180 TABLET in 1 BOTTLE (71335-3178-6)Marketed from Sep 24, 2026
71335-3178-7	71335317807	10 TABLET in 1 BOTTLE (71335-3178-7)Marketed from Sep 24, 2026

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
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077877
Marketing start: Dec 4, 2007
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 71335-3178_3aca509f-111d-4965-80f8-fefea17005b4SPL ID 3aca509f-111d-4965-80f8-fefea17005b4
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

N471335317801 followed by a unit qualifier and the quantity

Package 71335-3178-01. 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

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

About NDC 71335-3178

What is NDC 71335-3178?: 71335-3178 is the product NDC for Atenolol, Atenolol 100 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 7 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?: Bryant Ranch Prepack, NDC labeler code 71335. 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?: 123 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Atenolol	Atenolol 50 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-925	60760-0925-30
Atenolol	Atenolol 50 mg/1	TabletOral	Cardinal Health 107, LLC	55154-0283	55154-0283-00
Atenolol	Atenolol 100 mg/1	TabletOral	Coupler LLC	67046-1076	67046-1076-03
Atenolol	Atenolol 25 mg/1	TabletOral	Coupler LLC	67046-0663	67046-0663-03
Atenolol	Atenolol 50 mg/1	TabletOral	Coupler LLC	67046-0843	67046-0843-03
Atenolol	Atenolol 100 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4112	68788-4112-0168788-4112-0368788-4112-06+1 more
Atenolol	Atenolol 25 mg/1	TabletOral	Safecor Health, LLC	48433-004	48433-0004-20
Atenolol	Atenolol 50 mg/1	TabletOral	Safecor Health, LLC	48433-005	48433-0005-20
Atenolol	Atenolol 100 mg/1	TabletOral	Safecor Health, LLC	48433-006	48433-0006-20
Atenolol	Atenolol 50 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8834	68788-8834-0168788-8834-0368788-8834-06+1 more

All 124 Atenolol NDCs

Other NDCs under ANDA 077877

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

FDA NDC Directory listings under ANDA 077877
Product	Strength	Form · route	Labeler	Product NDC
Atenolol	Atenolol 100 mg/1	TabletOral	A-S Medication Solutions	50090-8048
Atenolol	Atenolol 25 mg/1	TabletOral	Ipca Laboratories Limited	83980-022
Atenolol	Atenolol 50 mg/1	TabletOral	Ipca Laboratories Limited	83980-023
Atenolol	Atenolol 100 mg/1	TabletOral	Ipca Laboratories Limited	83980-024