Prescription drug · ANDA
Atenolol NDC 50090-8048
Atenolol 100 mg/1 · Tablet · Oral · A-S Medication Solutions
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 50090-8048-0 | 50090804800 | 30 TABLET in 1 BOTTLE (50090-8048-0)Marketed from Sep 10, 2026 | |
| 50090-8048-3 | 50090804803 | 60 TABLET in 1 BOTTLE (50090-8048-3)Marketed from Sep 10, 2026 | |
| 50090-8048-5 | 50090804805 | 90 TABLET in 1 BOTTLE (50090-8048-5)Marketed from Sep 10, 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
- A-S Medication Solutions
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 077877
- Marketing start
- Listing expires
- Other FDA classes
- Adrenergic beta-Antagonists (Mechanism)
- Identifiers
- Product ID 50090-8048_bd3ee2fd-86f8-4290-a260-981529ea4ba2SPL ID bd3ee2fd-86f8-4290-a260-981529ea4ba2
- 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
N450090804800followed by a unit qualifier and the quantityPackage 50090-8048-00. 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.
Other NDCs under ANDA 077877
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.