Felodipine NDC 65862-674

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	65862067401	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-674-01)Marketed from Jan 17, 2013
65862-674-90	65862067490	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-674-90)Marketed from Jan 17, 2013
65862-674-99	65862067499	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 Limited
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 203417
Marketing start: Jan 17, 2013
Listing expires: Dec 31, 2026
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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

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	Aurobindo Pharma Limited	65862-673
Felodipine	Felodipine 10 mg/1	Tablet, Film coated, Extended releaseOral	Aurobindo Pharma Limited	65862-675
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 5 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	71335-1318