Prescription drug · ANDA
Quinapril NDC 68001-187
Quinapril hydrochloride 20 mg/1 · Tablet · Oral · BluePoint Laboratories
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 68001-187-05 | 68001018705 | 90 TABLET in 1 BOTTLE (68001-187-05)Marketed from Feb 25, 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)
- Quinapril
- Generic name (nonproprietary)
- quinapril
- Active ingredients
- Quinapril hydrochloride — 20 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- BluePoint Laboratories
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 077690
- Marketing start
- Listing expires
- Other FDA classes
- Angiotensin-converting Enzyme Inhibitors (Mechanism)
- Identifiers
- Product ID 68001-187_df08337a-79bd-47c9-858a-8ee32469cfe5SPL ID df08337a-79bd-47c9-858a-8ee32469cfe5SPL set ID 1b5809a8-873d-44cb-af59-e0d8fc81b385RxCUI 312748, 312749, 312750, 314203UNII 33067B3N2M
- 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
N468001018705followed by a unit qualifier and the quantityPackage 68001-0187-05. 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
Label details couldn’t be retrieved right now. Open the label on DailyMed.
Other NDCs under ANDA 077690
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 |
|---|---|---|---|---|
| Quinapril | Quinapril hydrochloride 10 mg/1 | TabletOral | Lupin Pharmaceuticals, Inc. | 68180-557 |
| Quinapril | Quinapril hydrochloride 40 mg/1 | TabletOral | Lupin Pharmaceuticals, Inc. | 68180-554 |
| Quinapril | Quinapril hydrochloride 20 mg/1 | TabletOral | Lupin Pharmaceuticals, Inc. | 68180-558 |
| Quinapril | Quinapril hydrochloride 40 mg/1 | TabletOral | Lupin Pharmaceuticals, Inc. | 68180-559 |
| Quinapril | Quinapril hydrochloride 10 mg/1 | TabletOral | Proficient Rx LP | 71205-635 |
| Quinapril | Quinapril hydrochloride 5 mg/1 | TabletOral | BluePoint Laboratories | 68001-189 |
| Quinapril | Quinapril hydrochloride 10 mg/1 | TabletOral | BluePoint Laboratories | 68001-188 |
| Quinapril | Quinapril hydrochloride 40 mg/1 | TabletOral | BluePoint Laboratories | 68001-260 |
| Quinapril | Quinapril hydrochloride 40 mg/1 | TabletOral | Northwind Health Company, LLC | 51655-737 |
| Quinapril | Quinapril hydrochloride 10 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-1707 |