What is NDC 62135-648?

62135-648 is the product NDC for Felodipine, Felodipine 10 mg/1 tablet, extended release, listed with the FDA by Chartwell RX, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Chartwell RX, LLC, NDC labeler code 62135. 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 62135-648 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)62135-648Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62135-0648Add 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
62135-648-90	6213506489062135064890	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (62135-648-90)Marketed from Jun 5, 2023

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 — 10 mg/1
Dosage form: Tablet, Extended release
Route: Oral
Labeler: Chartwell RX, LLCNDC labeler code 62135
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210847
Marketing start: Aug 1, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Calcium Channel Antagonists (Mechanism)Dihydropyridines (Chemical structure)
Identifiers: Product ID 62135-648_459bc915-c26d-844b-e063-6394a90a5c13SPL ID 459bc915-c26d-844b-e063-6394a90a5c13SPL set ID fddebfce-70ed-4ee1-8598-bbb8f1ca9263RxCUI 402695, 402696, 402698UNII OL961R6O2CUPC 0362135648909, 0362135646905, 0362135647902
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

N462135064890 followed by a unit qualifier and the quantity

Package 62135-0648-90. 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 Dec 10, 2025.

Full label on DailyMed (opens in a new tab)

About NDC 62135-648

What is NDC 62135-648?: 62135-648 is the product NDC for Felodipine, Felodipine 10 mg/1 tablet, extended release, listed with the FDA by Chartwell RX, LLC. 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?: Chartwell RX, LLC, NDC labeler code 62135. 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 210847

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

FDA NDC Directory listings under ANDA 210847
Product	Strength	Form · route	Labeler	Product NDC
Felodipine	Felodipine 2.5 mg/1	Tablet, Extended releaseOral	Chartwell RX, LLC	62135-646
Felodipine	Felodipine 5 mg/1	Tablet, Extended releaseOral	Chartwell RX, LLC	62135-647
Felodipinefelodipine extended-release tablets	Felodipine 2.5 mg/1	Tablet, Extended releaseOral	Yiling Pharmaceutical Inc.	69117-0028
Felodipinefelodipine extended-release tablets	Felodipine 5 mg/1	Tablet, Extended releaseOral	Yiling Pharmaceutical Inc.	69117-0029
Felodipinefelodipine extended-release tablets	Felodipine 10 mg/1	Tablet, Extended releaseOral	Yiling Pharmaceutical Inc.	69117-0030
Felodipine	Felodipine 2.5 mg/1	Tablet, Extended releaseOral	Westminster Pharmaceuticals, LLC	69367-264
Felodipine	Felodipine 5 mg/1	Tablet, Extended releaseOral	Westminster Pharmaceuticals, LLC	69367-265
Felopdipinefelodipine	Felodipine 10 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-7206
Felopdipinefelodipine	Felodipine 10 mg/1	Tablet, Extended releaseOral	Westminster Pharmaceuticals, LLC	69367-266