NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1431Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1431Add 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
71335-1431-1713351431017133514310130 TABLET in 1 BOTTLE (71335-1431-1)Marketed from Dec 6, 2019
71335-1431-2713351431027133514310290 TABLET in 1 BOTTLE (71335-1431-2)Marketed from May 30, 2024

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)
Trandolapril
Generic name (nonproprietary)
trandolapril
Active ingredients
Trandolapril — 2 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 71335
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078438
Marketing start
Listing expires
Other FDA classes
Angiotensin-converting Enzyme Inhibitors (Mechanism)
Identifiers
Product ID 71335-1431_43db4bac-8048-4f48-8325-4915515f31a4SPL ID 43db4bac-8048-4f48-8325-4915515f31a4SPL set ID 57f8aac6-3bd3-4ae1-aab2-759c8bc23292RxCUI 199351UNII 1T0N3G9CRC

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

N471335143101 followed by a unit qualifier and the quantity

Package 71335-1431-01. 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)

INDICATIONS AND USAGE Hypertension Trandolapril tablets USP are indicated for the treatment of hypertension. They may be used alone or in combination with other antihypertensive medication such as hydrochlorothiazide. Heart Failure Post Myocardial Infarction or Left-Ventricular Dysfunction Post Myocardial Infarction Trandolapril tablets USP are indicated in stable patients who have evidence of left-ventricular systolic dysfunction (identified by wall motion abnormalities) or who are symptomatic from congestive heart failure within the first few days after sustaining acute myocardial infarction. Administration of trandolapril to Caucasian patients has been shown to decrease the risk of death …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-1431

What is NDC 71335-1431?
71335-1431 is the product NDC for Trandolapril, Trandolapril 2 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Trandolapril.
What is the active ingredient?
Trandolapril.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Trandolapril?
12 other product NDCs are listed under this name. See all Trandolapril 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 Trandolapril NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Trandolapriltrandolapril tabletsTrandolapril 1 mg/1TabletOralEpic Pharma, LLC42806-05242806-0052-0142806-0052-10
Trandolapriltrandolapril tabletsTrandolapril 2 mg/1TabletOralEpic Pharma, LLC42806-05342806-0053-0142806-0053-10
Trandolapriltrandolapril tabletsTrandolapril 4 mg/1TabletOralEpic Pharma, LLC42806-05442806-0054-0142806-0054-10
TrandolaprilTrandolapril 1 mg/1TabletOralRising Pharma Holdings, Inc.57237-08957237-0089-01
TrandolaprilTrandolapril 2 mg/1TabletOralRising Pharma Holdings, Inc.57237-09057237-0090-01
TrandolaprilTrandolapril 4 mg/1TabletOralRising Pharma Holdings, Inc.57237-09157237-0091-01
TrandolaprilTrandolapril 1 mg/1TabletOralAurobindo Pharma Limited65862-16465862-0164-0165862-0164-99
TrandolaprilTrandolapril 2 mg/1TabletOralAurobindo Pharma Limited65862-16565862-0165-0165862-0165-99
TrandolaprilTrandolapril 2 mg/1TabletOralBryant Ranch Prepack63629-800363629-8003-0163629-8003-02
TrandolaprilTrandolapril 1 mg/1TabletOralLupin Pharmaceuticals, Inc.68180-56668180-0566-01

All 13 Trandolapril NDCs

Other NDCs under ANDA 078438

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

FDA NDC Directory listings under ANDA 078438
ProductStrengthForm · routeLabelerProduct NDC
TrandolaprilTrandolapril 1 mg/1TabletOralRising Pharma Holdings, Inc.57237-089
TrandolaprilTrandolapril 2 mg/1TabletOralRising Pharma Holdings, Inc.57237-090
TrandolaprilTrandolapril 4 mg/1TabletOralRising Pharma Holdings, Inc.57237-091
TrandolaprilTrandolapril 1 mg/1TabletOralAurobindo Pharma Limited65862-164
TrandolaprilTrandolapril 2 mg/1TabletOralAurobindo Pharma Limited65862-165

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