NDC codes

FDA NDC Directory
Product NDC (as listed)63629-2017Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63629-2017Add 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
63629-2017-163629201701500 TABLET, FILM COATED in 1 BOTTLE (63629-2017-1)Marketed from Oct 12, 2020

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, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 204800
Marketing start
Listing expires
Other FDA classes
Calcium Channel Antagonists (Mechanism)Dihydropyridines (Chemical structure)
Identifiers
Product ID 63629-2017_24a3c5d7-07a4-489e-8607-8c669b5211d9SPL ID 24a3c5d7-07a4-489e-8607-8c669b5211d9SPL set ID 5c7b7f9a-4f4c-4259-8aae-fdb91ab09eecRxCUI 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

N463629201701 followed by a unit qualifier and the quantity

Package 63629-2017-01. 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 204800

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

FDA NDC Directory listings under ANDA 204800
ProductStrengthForm · routeLabelerProduct NDC
FelodipineFelodipine 5 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-088
FelodipineFelodipine 10 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-089
FelodipineFelodipine 10 mg/1Tablet, Film coatedOralProficient Rx LP71205-922
FelodipineFelodipine 2.5 mg/1Tablet, Film coatedOralProficient Rx LP71205-920
FelodipineFelodipine 5 mg/1Tablet, Film coatedOralProficient Rx LP71205-921
FelodipineFelodipine 2.5 mg/1Tablet, Film coatedOralCarlsbad Technology, Inc.61442-431
FelodipineFelodipine 5 mg/1Tablet, Film coatedOralCarlsbad Technology, Inc.61442-432
FelodipineFelodipine 10 mg/1Tablet, Film coatedOralCarlsbad Technology, Inc.61442-433
FelodipineFelodipine 5 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2175
FelodipineFelodipine 10 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-2016
FelodipineFelodipine 5 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-2018
FelodipineFelodipine 5 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-1743
FelodipineFelodipine 2.5 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-1742
FelodipineFelodipine 10 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-1744

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