NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1486Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1486Add 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
71335-1486-1713351486017133514860130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1486-1)Marketed from Jan 21, 2020

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)
Felodipine
Generic name (nonproprietary)
felodipine
Active ingredients
Felodipine — 5 mg/1
Dosage form
Tablet, Film coated, Extended release
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 71335
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090365
Marketing start
Listing expires
Other FDA classes
Calcium Channel Antagonists (Mechanism)Dihydropyridines (Chemical structure)
Identifiers
Product ID 71335-1486_4d496596-33e4-4258-865f-fba7a00c39dfSPL ID 4d496596-33e4-4258-865f-fba7a00c39dfSPL set ID 924b2633-74bd-469f-b831-77f09dfebbf7RxCUI 402696UNII OL961R6O2C
Pharmacologic class
Dihydropyridine Calcium Channel Blocker

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

N471335148601 followed by a unit qualifier and the quantity

Package 71335-1486-01. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Felodipine tablets are indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure lowers the risk of fatal and non-fatal 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 felodipine. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will require more than 1 drug to achieve blood pressure g…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-1486

What is NDC 71335-1486?
71335-1486 is the product NDC for Felodipine, Felodipine 5 mg/1 tablet, film coated, extended release, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Felodipine.
What is the active ingredient?
Felodipine.
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 Felodipine?
49 other product NDCs are listed under this name. See all Felodipine 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 Felodipine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
FelodipineFelodipine 2.5 mg/1Tablet, Extended releaseOralWestminster Pharmaceuticals, LLC69367-26469367-0264-01
FelodipineFelodipine 5 mg/1Tablet, Extended releaseOralWestminster Pharmaceuticals, LLC69367-26569367-0265-01
FelodipineFelodipine 2.5 mg/1Tablet, Film coatedOralCarlsbad Technology, Inc.61442-43161442-0431-0161442-0431-05
FelodipineFelodipine 5 mg/1Tablet, Film coatedOralCarlsbad Technology, Inc.61442-43261442-0432-0161442-0432-05
FelodipineFelodipine 10 mg/1Tablet, Film coatedOralCarlsbad Technology, Inc.61442-43361442-0433-0161442-0433-05
FelodipineFelodipine 10 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-201663629-2016-01
FelodipineFelodipine 2.5 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-201763629-2017-01
FelodipineFelodipine 5 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-201863629-2018-01
FelodipineFelodipine 2.5 mg/1Tablet, Film coatedOralProficient Rx LP71205-92071205-0920-0071205-0920-3071205-0920-55+3 more
FelodipineFelodipine 5 mg/1Tablet, Film coatedOralProficient Rx LP71205-92171205-0921-0071205-0921-3071205-0921-55+3 more

All 50 Felodipine NDCs

Other NDCs under ANDA 090365

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

FDA NDC Directory listings under ANDA 090365
ProductStrengthForm · routeLabelerProduct NDC
FelodipineFelodipine 2.5 mg/1Tablet, Film coated, Extended releaseOralGlenmark Pharmaceuticals Inc., USA68462-233
FelodipineFelodipine 5 mg/1Tablet, Film coated, Extended releaseOralGlenmark Pharmaceuticals Inc., USA68462-234
FelodipineFelodipine 10 mg/1Tablet, Film coated, Extended releaseOralGlenmark Pharmaceuticals Inc., USA68462-235

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