What is NDC 65862-674?

65862-674 is the product NDC for Felodipine, Felodipine 5 mg/1 tablet, film coated, extended release, listed with the FDA by Aurobindo Pharma Limited. It has 3 package NDCs, shown above in 10- and 11-digit form.

Aurobindo Pharma Limited, NDC labeler code 65862. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Felodipine NDC 65862-674 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)65862-674Labeler and product segments. Claims need a package NDC.

Product NDC at billing width65862-0674Add 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 NDC	11-digit (billing)	Package
65862-674-01	6586206740165862067401	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-674-01)Marketed from Jan 17, 2013
65862-674-90	6586206749065862067490	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-674-90)Marketed from Jan 17, 2013
65862-674-99	6586206749965862067499	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-674-99)Marketed from Jan 17, 2013

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): Felodipine
Generic name (nonproprietary): felodipine
Active ingredients: Felodipine — 5 mg/1
Dosage form: Tablet, Film coated, Extended release
Route: Oral
Labeler: Aurobindo Pharma LimitedNDC labeler code 65862
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 203417
Marketing start: Jan 17, 2013
Listing expires: Dec 31, 2027
Other FDA classes: Calcium Channel Antagonists (Mechanism)Dihydropyridines (Chemical structure)
Identifiers: Product ID 65862-674_a8579789-363a-44b3-be60-fe7bad9b16a9SPL ID a8579789-363a-44b3-be60-fe7bad9b16a9SPL set ID dd39c559-5c5d-4d3b-9228-c44085e1699fRxCUI 402695, 402696, 402698UNII 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

N465862067401 followed by a unit qualifier and the quantity

Package 65862-0674-01. 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 Feb 17, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Felodipine extended-release tablets, USP 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 ac…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 65862-674

What is NDC 65862-674?: 65862-674 is the product NDC for Felodipine, Felodipine 5 mg/1 tablet, film coated, extended release, listed with the FDA by Aurobindo Pharma Limited. It has 3 package NDCs, 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?: Aurobindo Pharma Limited, NDC labeler code 65862. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Felodipine	Felodipine 2.5 mg/1	Tablet, Extended releaseOral	Westminster Pharmaceuticals, LLC	69367-264	69367-0264-01
Felodipine	Felodipine 5 mg/1	Tablet, Extended releaseOral	Westminster Pharmaceuticals, LLC	69367-265	69367-0265-01
Felodipine	Felodipine 2.5 mg/1	Tablet, Film coatedOral	Carlsbad Technology, Inc.	61442-431	61442-0431-0161442-0431-05
Felodipine	Felodipine 5 mg/1	Tablet, Film coatedOral	Carlsbad Technology, Inc.	61442-432	61442-0432-0161442-0432-05
Felodipine	Felodipine 10 mg/1	Tablet, Film coatedOral	Carlsbad Technology, Inc.	61442-433	61442-0433-0161442-0433-05
Felodipine	Felodipine 10 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-2016	63629-2016-01
Felodipine	Felodipine 2.5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-2017	63629-2017-01
Felodipine	Felodipine 5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-2018	63629-2018-01
Felodipine	Felodipine 2.5 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-920	71205-0920-0071205-0920-3071205-0920-55+3 more
Felodipine	Felodipine 5 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-921	71205-0921-0071205-0921-3071205-0921-55+3 more

All 50 Felodipine NDCs

Other NDCs under ANDA 203417

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

FDA NDC Directory listings under ANDA 203417
Product	Strength	Form · route	Labeler	Product NDC
Felodipine	Felodipine 10 mg/1	Tablet, Film coated, Extended releaseOral	A-S Medication Solutions	50090-5870
Felodipine	Felodipine 2.5 mg/1	Tablet, Film coated, Extended releaseOral	Rising Pharma Holdings, Inc.	57237-108
Felodipine	Felodipine 5 mg/1	Tablet, Film coated, Extended releaseOral	Rising Pharma Holdings, Inc.	57237-109
Felodipine	Felodipine 10 mg/1	Tablet, Film coated, Extended releaseOral	Rising Pharma Holdings, Inc.	57237-110
Felodipine	Felodipine 2.5 mg/1	Tablet, Film coated, Extended releaseOral	Aurobindo Pharma Limited	65862-673
Felodipine	Felodipine 5 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	71335-1318