NDC codes

FDA NDC Directory
Product NDC (as listed)43547-412Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43547-0412Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
43547-412-094354704120990 TABLET in 1 BOTTLE (43547-412-09)Marketed from Nov 10, 2017

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
Solco Healthcare US, LLCNDC labeler code 43547
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 205823
Marketing start
Listing expires
Other FDA classes
Angiotensin-converting Enzyme Inhibitors (Mechanism)
Identifiers
Product ID 43547-412_b8f1731a-cbac-4f64-a8d4-320b80b335e1SPL ID b8f1731a-cbac-4f64-a8d4-320b80b335e1SPL set ID cd46691d-5593-4a9f-a937-999c6803e312RxCUI 312748, 312749, 312750, 314203UNII 33067B3N2M

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

N443547041209 followed by a unit qualifier and the quantity

Package 43547-0412-09. 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)

INDICATIONS AND USAGE Hypertension Quinapril 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. There are no controlled trials demonstrating risk reduction with quinapril tablets. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic th…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43547-412

What is NDC 43547-412?
43547-412 is the product NDC for Quinapril, Quinapril hydrochloride 20 mg/1 tablet, listed with the FDA by Solco Healthcare US, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Quinapril.
What is the active ingredient?
Quinapril hydrochloride.
Who is the labeler?
Solco Healthcare US, LLC, NDC labeler code 43547. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Quinapril?
30 other product NDCs are listed under this name. See all Quinapril NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Quinapril NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
QuinaprilQuinapril hydrochloride 40 mg/1TabletOralNorthwind Health Company, LLC51655-73751655-0737-52
QuinaprilQuinapril hydrochloride 5 mg/1TabletOralSolco Healthcare US, LLC43547-41043547-0410-09
QuinaprilQuinapril hydrochloride 10 mg/1TabletOralSolco Healthcare US, LLC43547-41143547-0411-09
QuinaprilQuinapril hydrochloride 20 mg/1TabletOralBryant Ranch Prepack63629-871063629-8710-01
QuinaprilQuinapril hydrochloride 10 mg/1TabletOralProficient Rx LP71205-48471205-0484-3071205-0484-6071205-0484-90
QuinaprilQuinapril hydrochloride 10 mg/1TabletOralBryant Ranch Prepack71335-113471335-1134-01
QuinaprilQuinapril hydrochloride 5 mg/1TabletOralCipla USA Inc.69097-83969097-0839-0569097-0839-15
QuinaprilQuinapril hydrochloride 10 mg/1TabletOralCipla USA Inc.69097-84169097-0841-0569097-0841-15
QuinaprilQuinapril hydrochloride 20 mg/1TabletOralCipla USA Inc.69097-84269097-0842-0569097-0842-15
QuinaprilQuinapril hydrochloride 40 mg/1TabletOralCipla USA Inc.69097-84369097-0843-0569097-0843-15

All 31 Quinapril NDCs

Other NDCs under ANDA 205823

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 205823
ProductStrengthForm · routeLabelerProduct NDC
QuinaprilQuinapril hydrochloride 5 mg/1TabletOralSolco Healthcare US, LLC43547-410
QuinaprilQuinapril hydrochloride 10 mg/1TabletOralSolco Healthcare US, LLC43547-411
QuinaprilQuinapril hydrochloride 40 mg/1TabletOralSolco Healthcare US, LLC43547-413
QuinaprilQuinapril hydrochloride 20 mg/1TabletOralBryant Ranch Prepack63629-8710
QuinaprilQuinapril hydrochloride 10 mg/1TabletOralProficient Rx LP71205-484
QuinaprilQuinapril hydrochloride 10 mg/1TabletOralBryant Ranch Prepack71335-1134

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