Prescription drug · NDA
Qbrelis (Lisinopril) NDC 52652-3001
Lisinopril 1 mg/mL · Solution · Oral · Azurity Pharmaceuticals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 52652-3001-1 | 52652300101 | 150 mL in 1 BOTTLE (52652-3001-1)Marketed from Aug 29, 2016 |
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)
- Qbrelis
- Generic name (nonproprietary)
- lisinopril
- Active ingredients
- Lisinopril — 1 mg/mL
- Dosage form
- Solution
- Route
- Oral
- Labeler
- Azurity Pharmaceuticals, Inc.NDC labeler code 52652
- Product type
- Prescription drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 208401
- Marketing start
- Listing expires
- Other FDA classes
- Angiotensin-converting Enzyme Inhibitors (Mechanism)
- Identifiers
- Product ID 52652-3001_461e97d5-c8b3-75a7-e063-6394a90a6ec6SPL ID 461e97d5-c8b3-75a7-e063-6394a90a6ec6SPL set ID 9f6e4e57-a489-4b36-b093-b93865d3717cRxCUI 1806884, 1806890UNII E7199S1YWR
- 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
N452652300101followed by a unit qualifier and the quantityPackage 52652-3001-01. 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 . This label includes a boxed warning.
Indications (excerpt from the label)
QBRELIS is an angiotensin converting enzyme (ACE) inhibitor indicated for: Treatment of hypertension in adults and pediatric patients 6 years of age and older ( 1.1 ). Adjunct therapy for heart failure ( 1.2 ). Treatment of Acute Myocardial Infarction ( 1.3 ). 1.1 Hypertension QBRELIS is indicated for the treatment of hypertension in adult patients and pediatric patients 6 years of age and older to lower blood pressure. Lowering blood pressure lowers 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. Control of high blood …
Excerpt only. Read the full label for complete information.
About NDC 52652-3001
- What is NDC 52652-3001?
- 52652-3001 is the product NDC for Qbrelis (lisinopril), Lisinopril 1 mg/mL solution, listed with the FDA by Azurity Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Qbrelis (Lisinopril).
- What is the active ingredient?
- Lisinopril.
- Who is the labeler?
- Azurity Pharmaceuticals, Inc., NDC labeler code 52652. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Qbrelis?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.