What is NDC 72162-2568?

72162-2568 is the product NDC for Felodipine, Felodipine 2.5 mg/1 tablet, extended release, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 72162. 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 72162-2568 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72162-2568Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72162-2568Add 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	Copy
72162-2568-1	7216225680172162256801	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2568-1)Marketed from Nov 17, 2025

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 — 2.5 mg/1
Dosage form: Tablet, Extended release
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 72162
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202170
Marketing start: Nov 28, 2011
Listing expires: Dec 31, 2026
Other FDA classes: Calcium Channel Antagonists (Mechanism)Dihydropyridines (Chemical structure)
Identifiers: Product ID 72162-2568_7068c99c-1af6-49b7-8157-82786539576fSPL ID 7068c99c-1af6-49b7-8157-82786539576fSPL set ID 57fb4217-00f6-4112-bc63-81fcbe2ea903RxCUI 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

N472162256801 followed by a unit qualifier and the quantity

Package 72162-2568-01. 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 Nov 17, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Felodipine extended-release tablets are indicated for the treatment of hypertension. Felodipine extended-release tablets may be used alone or concomitantly with other antihypertensive agents.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-2568

What is NDC 72162-2568?: 72162-2568 is the product NDC for Felodipine, Felodipine 2.5 mg/1 tablet, 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 72162. 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 202170

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

FDA NDC Directory listings under ANDA 202170
Product	Strength	Form · route	Labeler	Product NDC
Felodipine	Felodipine 10 mg/1	Tablet, Extended releaseOral	Torrent Pharmaceuticals Limited	13668-134
Felodipine	Felodipine 2.5 mg/1	Tablet, Extended releaseOral	Torrent Pharmaceuticals Limited	13668-132
Felodipine	Felodipine 5 mg/1	Tablet, Extended releaseOral	Torrent Pharmaceuticals Limited	13668-133
Felodipine	Felodipine 10 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-1124