NDC codes

FDA NDC Directory
Product NDC (as listed)62135-647Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62135-0647Add 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
62135-647-906213506479090 TABLET, EXTENDED RELEASE in 1 BOTTLE (62135-647-90)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 — 5 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 210847
Marketing start
Listing expires
Other FDA classes
Calcium Channel Antagonists (Mechanism)Dihydropyridines (Chemical structure)
Identifiers
Product ID 62135-647_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

N462135064790 followed by a unit qualifier and the quantity

Package 62135-0647-90. 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 .

Full label on DailyMed (opens in a new tab)

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
ProductStrengthForm · routeLabelerProduct NDC
Felodipinefelodipine extended-release tabletsFelodipine 5 mg/1Tablet, Extended releaseOralYiling Pharmaceutical Inc.69117-0029
Felodipinefelodipine extended-release tabletsFelodipine 2.5 mg/1Tablet, Extended releaseOralYiling Pharmaceutical Inc.69117-0028
Felodipinefelodipine extended-release tabletsFelodipine 10 mg/1Tablet, Extended releaseOralYiling Pharmaceutical Inc.69117-0030
FelopdipinefelodipineFelodipine 10 mg/1Tablet, Extended releaseOralA-S Medication Solutions50090-7206
FelodipineFelodipine 2.5 mg/1Tablet, Extended releaseOralChartwell RX, LLC62135-646
FelodipineFelodipine 10 mg/1Tablet, Extended releaseOralChartwell RX, LLC62135-648
FelodipineFelodipine 2.5 mg/1Tablet, Extended releaseOralWestminster Pharmaceuticals, LLC69367-264
FelodipineFelodipine 5 mg/1Tablet, Extended releaseOralWestminster Pharmaceuticals, LLC69367-265
FelopdipinefelodipineFelodipine 10 mg/1Tablet, Extended releaseOralWestminster Pharmaceuticals, LLC69367-266

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Felodipine NDC 62135-647 | Med-Code