Prescription drug · ANDA
Benazepril Hydrochloride NDC 68071-3057
Benazepril hydrochloride 10 mg/1 · Tablet, Coated · Oral · NuCare Pharmaceuticals,Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 68071-3057-2 | 68071305702 | 120 TABLET, COATED in 1 BOTTLE (68071-3057-2)Marketed from Aug 2, 2018 | |
| 68071-3057-3 | 68071305703 | 30 TABLET, COATED in 1 BOTTLE (68071-3057-3)Marketed from Aug 2, 2018 | |
| 68071-3057-6 | 68071305706 | 60 TABLET, COATED in 1 BOTTLE (68071-3057-6)Marketed from Aug 2, 2018 | |
| 68071-3057-9 | 68071305709 | 90 TABLET, COATED in 1 BOTTLE (68071-3057-9)Marketed from Aug 2, 2018 |
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)
- Benazepril Hydrochloride
- Generic name (nonproprietary)
- benazepril hydrochloride
- Active ingredients
- Benazepril hydrochloride — 10 mg/1
- Dosage form
- Tablet, Coated
- Route
- Oral
- Labeler
- NuCare Pharmaceuticals,Inc.
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 076118
- Marketing start
- Listing expires
- Other FDA classes
- Angiotensin-converting Enzyme Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)
- Identifiers
- Product ID 68071-3057_1d8e646c-3666-431e-e063-6394a90a34e4SPL ID 1d8e646c-3666-431e-e063-6394a90a34e4SPL set ID 7274fdaf-1247-2b2f-e053-2991aa0ad3f6RxCUI 898687UNII N1SN99T69TUPC 0368071305739
- 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
N468071305702followed by a unit qualifier and the quantityPackage 68071-3057-02. 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 hydrochloride 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 …
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 076118
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 20 mg/1 | Tablet, CoatedOral | Northwind Health Company, LLC | 51655-066 |
| Benazepril Hydrochloride | Benazepril hydrochloride 20 mg/1 | Tablet, CoatedOral | A-S Medication Solutions | 50090-3243 |
| Benazepril Hydrochloride | Benazepril hydrochloride 10 mg/1 | Tablet, CoatedOral | Northwind Health Company, LLC | 51655-065 |
| Benazepril Hydrochloride | Benazepril hydrochloride 20 mg/1 | Tablet, CoatedOral | NuCare Pharmaceuticals,Inc. | 68071-1969 |
| Benazepril Hydrochloride | Benazepril hydrochloride 5 mg/1 | Tablet, CoatedOral | Preferred Pharmaceuticals Inc. | 68788-6889 |
| Benazepril Hydrochloride | Benazepril hydrochloride 40 mg/1 | Tablet, CoatedOral | Preferred Pharmaceuticals Inc. | 68788-6957 |
| Benazepril Hydrochloride | Benazepril hydrochloride 10 mg/1 | Tablet, CoatedOral | DIRECT RX | 72189-110 |
| Benazepril Hydrochloride | Benazepril hydrochloride 5 mg/1 | Tablet, CoatedOral | NuCare Pharmaceuticals,Inc. | 68071-5130 |
| Benazepril Hydrochloride | Benazepril hydrochloride 10 mg/1 | Tablet, CoatedOral | NuCare Pharmaceuticals,Inc. | 68071-5129 |
| Benazepril Hydrochloride | Benazepril hydrochloride 40 mg/1 | Tablet, CoatedOral | REMEDYREPACK INC. | 70518-2125 |
| Benazepril Hydrochloride | Benazepril hydrochloride 10 mg/1 | Tablet, CoatedOral | Bryant Ranch Prepack | 71335-0457 |
| Benazepril Hydrochloride | Benazepril hydrochloride 40 mg/1 | Tablet, CoatedOral | A-S Medication Solutions | 50090-0914 |
| Benazepril Hydrochloride | Benazepril hydrochloride 5 mg/1 | Tablet, CoatedOral | NuCare Pharmaceuticals, Inc. | 68071-3324 |
| Benazepril Hydrochloride | Benazepril hydrochloride 20 mg/1 | Tablet, CoatedOral | Proficient Rx LP | 63187-393 |
| Benazepril Hydrochloride | Benazepril hydrochloride 40 mg/1 | Tablet, CoatedOral | Northwind Health Company, LLC | 82868-089 |
| Benazepril Hydrochloride | Benazepril hydrochloride 20 mg/1 | Tablet, CoatedOral | Preferred Pharmaceuticals, Inc. | 68788-9313 |
| Benazepril Hydrochloride | Benazepril hydrochloride 10 mg/1 | Tablet, CoatedOral | Preferred Pharmaceuticals, Inc. | 68788-9327 |
| Benazepril Hydrochloride | Benazepril hydrochloride 20 mg/1 | Tablet, CoatedOral | Bryant Ranch Prepack | 71335-0078 |
| Benazepril Hydrochloride | Benazepril hydrochloride 20 mg/1 | Tablet, CoatedOral | Solco healthcare U.S., LLC | 43547-337 |
| Benazepril Hydrochloride | Benazepril hydrochloride 5 mg/1 | Tablet, CoatedOral | Solco healthcare U.S., LLC | 43547-335 |
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