Prescription drug · ANDA
Atenolol NDC 65841-023
Atenolol 50 mg/1 · Tablet · Oral · Zydus Lifesciences Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 65841-023-01 | 65841002301 | 100 TABLET in 1 BOTTLE (65841-023-01)Marketed from Oct 8, 2005 | |
| 65841-023-02 | 65841002302 | 2000 TABLET in 1 BOTTLE (65841-023-02)Marketed from Oct 8, 2005 | |
| 65841-023-10 | 65841002310 | 1000 TABLET in 1 BOTTLE (65841-023-10)Marketed from Oct 8, 2005 | |
| 65841-023-16 | 65841002316 | 90 TABLET in 1 BOTTLE (65841-023-16)Marketed from Oct 8, 2005 | |
| 65841-023-24 | 65841002324 | 10000 TABLET in 1 BOTTLE (65841-023-24)Marketed from Oct 8, 2005 | |
| 65841-023-40 | 65841002340 | 5000 TABLET in 1 BOTTLE (65841-023-40)Marketed from Oct 8, 2005 |
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 — 50 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Zydus Lifesciences Limited
- 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 65841-023_f4fb6b85-6379-4e8a-9ee3-402819d128a0SPL ID f4fb6b85-6379-4e8a-9ee3-402819d128a0SPL set ID 2492d5f6-00b0-42c9-a793-2be83ea81ad1RxCUI 197379, 197380, 197381UNII 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
N465841002301followed by a unit qualifier and the quantityPackage 65841-0023-01. 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 .
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 50 mg/1 | TabletOral | A-S Medication Solutions | 50090-6779 |
| Atenolol | Atenolol 25 mg/1 | TabletOral | American Health Packaging | 60687-605 |
| Atenolol | Atenolol 25 mg/1 | TabletOral | PD-Rx Pharmaceuticals, Inc. | 43063-952 |
| 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 | PD-Rx Pharmaceuticals, Inc. | 72789-144 |
| Atenolol | Atenolol 100 mg/1 | TabletOral | Zydus Lifesciences Limited | 65841-024 |
| Atenolol | Atenolol 25 mg/1 | TabletOral | Zydus Lifesciences Limited | 65841-022 |
| Atenolol | Atenolol 100 mg/1 | TabletOral | NuCare Pharmaceuticals, Inc. | 66267-029 |
| Atenolol | Atenolol 50 mg/1 | TabletOral | A-S Medication Solutions | 50090-0442 |
| Atenolol | Atenolol 50 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-0912 |