NDC codes

FDA NDC Directory
Product NDC (as listed)68001-260Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68001-0260Add 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
68001-260-056800102600590 TABLET in 1 BOTTLE (68001-260-05)Marketed from Jul 18, 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 — 40 mg/1
Dosage form
Tablet
Route
Oral
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 68001-260_df08337a-79bd-47c9-858a-8ee32469cfe5SPL ID df08337a-79bd-47c9-858a-8ee32469cfe5SPL set ID 1b5809a8-873d-44cb-af59-e0d8fc81b385RxCUI 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

N468001026005 followed by a unit qualifier and the quantity

Package 68001-0260-05. 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.

FDA NDC Directory listings under ANDA 077690
ProductStrengthForm · routeLabelerProduct NDC
QuinaprilQuinapril hydrochloride 10 mg/1TabletOralLupin Pharmaceuticals, Inc.68180-557
QuinaprilQuinapril hydrochloride 40 mg/1TabletOralLupin Pharmaceuticals, Inc.68180-554
QuinaprilQuinapril hydrochloride 20 mg/1TabletOralLupin Pharmaceuticals, Inc.68180-558
QuinaprilQuinapril hydrochloride 40 mg/1TabletOralLupin Pharmaceuticals, Inc.68180-559
QuinaprilQuinapril hydrochloride 10 mg/1TabletOralProficient Rx LP71205-635
QuinaprilQuinapril hydrochloride 5 mg/1TabletOralBluePoint Laboratories68001-189
QuinaprilQuinapril hydrochloride 20 mg/1TabletOralBluePoint Laboratories68001-187
QuinaprilQuinapril hydrochloride 10 mg/1TabletOralBluePoint Laboratories68001-188
QuinaprilQuinapril hydrochloride 40 mg/1TabletOralNorthwind Health Company, LLC51655-737
QuinaprilQuinapril hydrochloride 10 mg/1TabletOralBryant Ranch Prepack71335-1707

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