Prescription drug · ANDA
Benazepril Hydrochloride NDC 50268-112
Benazepril hydrochloride 40 mg/1 · Tablet · Oral · AvPAK
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 50268-112-15 | 50268011215 | 50 BLISTER PACK in 1 BOX (50268-112-15) / 1 TABLET in 1 BLISTER PACK (50268-112-11)Marketed from Apr 28, 2014 |
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)
- Benazepril Hydrochloride
- Generic name (nonproprietary)
- benazepril hydrochloride
- Active ingredients
- Benazepril hydrochloride — 40 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- AvPAK
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 076820
- Marketing start
- Listing expires
- Other FDA classes
- Angiotensin-converting Enzyme Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)
- Identifiers
- Product ID 50268-112_3f7e3955-e107-517a-e063-6294a90a0b13SPL ID 3f7e3955-e107-517a-e063-6294a90a0b13SPL set ID f004d7e2-fc45-8a37-e548-eeaaa327f9b5RxCUI 898687, 898690, 898719, 898723UNII N1SN99T69T
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
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
N450268011215followed by a unit qualifier and the quantityPackage 50268-0112-15. 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)
Benazepril HCl tablets are 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. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including the class to which this drug principally belongs. 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 one drug to ac…
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 076820
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 |
|---|---|---|---|---|
| Benazepril Hydrochloride | Benazepril hydrochloride 5 mg/1 | TabletOral | Amneal Pharmaceuticals LLC | 65162-751 |
| Benazepril Hydrochloride | Benazepril hydrochloride 10 mg/1 | TabletOral | Amneal Pharmaceuticals LLC | 65162-752 |
| Benazepril Hydrochloride | Benazepril hydrochloride 20 mg/1 | TabletOral | Amneal Pharmaceuticals LLC | 65162-753 |
| Benazepril Hydrochloride | Benazepril hydrochloride 40 mg/1 | TabletOral | Amneal Pharmaceuticals LLC | 65162-754 |
| Benazepril Hydrochloride | Benazepril hydrochloride 20 mg/1 | TabletOral | Cardinal Health 107, LLC | 55154-4344 |
| Benazepril Hydrochloride | Benazepril hydrochloride 10 mg/1 | TabletOral | Cardinal Health 107, LLC | 55154-4343 |
| Benazepril Hydrochloride | Benazepril hydrochloride 20 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-1086 |
| Benazepril Hydrochloride | Benazepril hydrochloride 10 mg/1 | TabletOral | AvPAK | 50268-110 |
| Benazepril Hydrochloride | Benazepril hydrochloride 5 mg/1 | TabletOral | AvPAK | 50268-109 |
| Benazepril Hydrochloride | Benazepril hydrochloride 20 mg/1 | TabletOral | AvPAK | 50268-111 |
| Benazepril Hydrochloride | Benazepril hydrochloride 10 mg/1 | TabletOral | Bryant Ranch Prepack | 72162-1816 |
| Benazepril Hydrochloride | Benazepril hydrochloride 20 mg/1 | TabletOral | Northwind Health Company, LLC | 51655-755 |
| Benazepril Hydrochloride | Benazepril hydrochloride 20 mg/1 | TabletOral | Proficient Rx LP | 71205-244 |
| Benazepril Hydrochloride | Benazepril hydrochloride 20 mg/1 | TabletOral | Amneal Pharmaceuticals of New York LLC | 53746-753 |
| Benazepril Hydrochloride | Benazepril hydrochloride 5 mg/1 | TabletOral | Amneal Pharmaceuticals of New York LLC | 53746-751 |
| Benazepril Hydrochloride | Benazepril hydrochloride 10 mg/1 | TabletOral | Amneal Pharmaceuticals of New York LLC | 53746-752 |
| Benazepril Hydrochloride | Benazepril hydrochloride 40 mg/1 | TabletOral | Amneal Pharmaceuticals of New York LLC | 53746-754 |
| Benazepril Hydrochloride | Benazepril hydrochloride 10 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-0854 |
- openFDA data updated
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