Prescription drug · ANDA
Atenolol NDC 60687-605
Atenolol 25 mg/1 · Tablet · Oral · American Health Packaging
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 60687-605-01 | 6068706050160687060501 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-605-01) / 1 TABLET in 1 BLISTER PACK (60687-605-11)Marketed from Oct 25, 2021 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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
- Labeler
- American Health PackagingNDC labeler code 60687
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 076900
- Marketing start
- Listing expires
- Other FDA classes
- Adrenergic beta-Antagonists (Mechanism)
- Identifiers
- Product ID 60687-605_29ba4e19-11d5-b7fb-e063-6394a90a9fafSPL ID 29ba4e19-11d5-b7fb-e063-6394a90a9fafSPL set ID d19e9fcf-dfa1-43d7-94dc-e3f03fb90f5cRxCUI 197380UNII 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
N460687060501followed by a unit qualifier and the quantityPackage 60687-0605-01. 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 . This label includes a boxed warning.
Indications (excerpt from the label)
INDICATIONS AND USAGE Hypertension Atenolol is 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 pressure g…
Excerpt only. Read the full label for complete information.
About NDC 60687-605
- What is NDC 60687-605?
- 60687-605 is the product NDC for Atenolol, Atenolol 25 mg/1 tablet, listed with the FDA by American Health Packaging. It has 1 package NDC, 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?
- American Health Packaging, NDC labeler code 60687. 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.
Related NDCs: other Atenolol products
Other finished products listed under the same name: strengths, forms and labelers.
| 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 100 mg/1 | TabletOral | Safecor Health, LLC | 48433-006 | 48433-0006-20 |
| 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 50 mg/1 | TabletOral | Preferred Pharmaceuticals Inc. | 68788-8834 | 68788-8834-0168788-8834-0368788-8834-06+1 more |
Other NDCs under ANDA 076900
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Atenolol | Atenolol 25 mg/1 | TabletOral | PD-Rx Pharmaceuticals, Inc. | 43063-952 |
| Atenolol | Atenolol 50 mg/1 | TabletOral | PD-Rx Pharmaceuticals, Inc. | 72789-144 |
| Atenolol | Atenolol 50 mg/1 | TabletOral | A-S Medication Solutions | 50090-6779 |
| Atenolol | Atenolol 50 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-0912 |
| Atenolol | Atenolol 25 mg/1 | TabletOral | Zydus Pharmaceuticals USA Inc. | 68382-022 |
| Atenolol | Atenolol 50 mg/1 | TabletOral | Zydus Pharmaceuticals USA Inc. | 68382-023 |
| Atenolol | Atenolol 100 mg/1 | TabletOral | Zydus Pharmaceuticals USA Inc. | 68382-024 |
| Atenolol | Atenolol 50 mg/1 | TabletOral | A-S Medication Solutions | 50090-0442 |
| Atenolol | Atenolol 50 mg/1 | TabletOral | Zydus Lifesciences Limited | 65841-023 |
| Atenolol | Atenolol 25 mg/1 | TabletOral | Zydus Lifesciences Limited | 65841-022 |
| Atenolol | Atenolol 100 mg/1 | TabletOral | Zydus Lifesciences Limited | 65841-024 |
| Atenolol | Atenolol 100 mg/1 | TabletOral | NuCare Pharmaceuticals, Inc. | 66267-029 |