Prescription drug · ANDA
Nebivolol NDC 60687-641
Nebivolol hydrochloride 5 mg/1 · Tablet · Oral · American Health Packaging
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 60687-641-21 | 6068706412160687064121 | 30 BLISTER PACK in 1 CARTON (60687-641-21) / 1 TABLET in 1 BLISTER PACK (60687-641-11)Marketed from Sep 7, 2022 |
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)
- Nebivolol
- Generic name (nonproprietary)
- nebivolol
- Active ingredients
- Nebivolol hydrochloride — 5 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 203828
- Marketing start
- Listing expires
- Other FDA classes
- Adrenergic beta-Antagonists (Mechanism)
- Identifiers
- Product ID 60687-641_35420d8c-7a05-0220-e063-6394a90a1c25SPL ID 35420d8c-7a05-0220-e063-6394a90a1c25SPL set ID 5418f2b2-3e23-4e7a-b4df-36a1515c9a12RxCUI 387013, 751612UNII JGS34J7L9I
- 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
N460687064121followed by a unit qualifier and the quantityPackage 60687-0641-21. 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 .
Indications (excerpt from the label)
Nebivolol is a beta-adrenergic blocking agent indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. (1.1) 1.1 Hypertension Nebivolol tablets are indicated for the treatment of hypertension, to lower blood pressure [see Clinical Studies (14.1) ]. Nebivolol tablets may be used alone or in combination with other antihypertensive agents [see Drug Interactions (7) ]. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of a…
Excerpt only. Read the full label for complete information.
About NDC 60687-641
- What is NDC 60687-641?
- 60687-641 is the product NDC for Nebivolol, Nebivolol hydrochloride 5 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?
- Nebivolol.
- What is the active ingredient?
- Nebivolol hydrochloride.
- 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 Nebivolol?
- 89 other product NDCs are listed under this name. See all Nebivolol NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Nebivolol products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Nebivolol | Nebivolol 20 mg/1 | TabletOral | Major Pharmaceuticals | 0904-7500 | 00904-7500-04 |
| Nebivolol | Nebivolol hydrochloride 5 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4648 | 70518-4648-00 |
| Nebivolol | Nebivolol hydrochloride 2.5 mg/1 | TabletOral | NorthStar RxLLC | 72603-870 | 72603-0870-01 |
| Nebivolol | Nebivolol hydrochloride 5 mg/1 | TabletOral | NorthStar RxLLC | 72603-871 | 72603-0871-0172603-0871-02 |
| Nebivolol | Nebivolol hydrochloride 10 mg/1 | TabletOral | NorthStar RxLLC | 72603-872 | 72603-0872-0172603-0872-02 |
| Nebivolol | Nebivolol hydrochloride 20 mg/1 | TabletOral | NorthStar RxLLC | 72603-873 | 72603-0873-0172603-0873-02 |
| Nebivolol | Nebivolol 2.5 mg/1 | TabletOral | Major Pharmaceuticals | 0904-7497 | 00904-7497-04 |
| Nebivolol | Nebivolol 5 mg/1 | TabletOral | Major Pharmaceuticals | 0904-7498 | 00904-7498-04 |
| Nebivolol | Nebivolol 10 mg/1 | TabletOral | Major Pharmaceuticals | 0904-7499 | 00904-7499-04 |
| Nebivolol | Nebivolol hydrochloride 2.5 mg/1 | TabletOral | Macleods Pharmaceuticals Limited | 33342-457 | 33342-0457-0733342-0457-1033342-0457-25 |
Other NDCs under ANDA 203828
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 |
|---|---|---|---|---|
| Nebivolol | Nebivolol hydrochloride 2.5 mg/1 | TabletOral | A-S Medication Solutions | 50090-5708 |
| Nebivolol | Nebivolol hydrochloride 5 mg/1 | TabletOral | A-S Medication Solutions | 50090-5752 |
| Nebivolol | Nebivolol hydrochloride 10 mg/1 | TabletOral | A-S Medication Solutions | 50090-5761 |
| Nebivolol | Nebivolol hydrochloride 10 mg/1 | TabletOral | American Health Packaging | 60687-652 |
| Nebivolol | Nebivolol hydrochloride 20 mg/1 | TabletOral | Ascend Laboratories, LLC | 67877-390 |
| Nebivolol | Nebivolol hydrochloride 10 mg/1 | TabletOral | Ascend Laboratories, LLC | 67877-391 |
| Nebivolol | Nebivolol hydrochloride 5 mg/1 | TabletOral | Ascend Laboratories, LLC | 67877-392 |
| Nebivolol | Nebivolol hydrochloride 2.5 mg/1 | TabletOral | Ascend Laboratories, LLC | 67877-393 |
| Nebivolol | Nebivolol hydrochloride 5 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-3527 |