Fenofibrate NDC 62332-084

NDC codes

FDA NDC Directory

Product NDC (as listed)62332-084Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62332-0084Add 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
62332-084-30	62332008430	30 CAPSULE in 1 BOTTLE (62332-084-30)Marketed from Oct 22, 2020
62332-084-31	62332008431	100 CAPSULE in 1 BOTTLE (62332-084-31)Marketed from Oct 22, 2020
62332-084-71	62332008471	500 CAPSULE in 1 BOTTLE (62332-084-71)Marketed from Oct 22, 2020

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): Fenofibrate
Generic name (nonproprietary): fenofibrate
Active ingredients: Fenofibrate — 67 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Alembic Pharmaceuticals Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213842
Marketing start: Oct 22, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 62332-084_855b1ec7-573c-417c-8485-0b36f728feafSPL ID 855b1ec7-573c-417c-8485-0b36f728feafSPL set ID d5c046b5-c3fd-4ef3-8245-c93796d4d880RxCUI 200311, 310288, 310289UNII U202363UOSUPC 0362332086306, 0362332085309, 0362332084302
Pharmacologic class: Peroxisome Proliferator Receptor alpha Agonist

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

N462332008430 followed by a unit qualifier and the quantity

Package 62332-0084-30. 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 213842

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

FDA NDC Directory listings under ANDA 213842
Product	Strength	Form · route	Labeler	Product NDC
Fenofibrate	Fenofibrate 200 mg/1	CapsuleOral	A-S Medication Solutions	50090-7994
Fenofibrate	Fenofibrate 67 mg/1	CapsuleOral	Alembic Pharmaceuticals Limited	46708-084
Fenofibrate	Fenofibrate 134 mg/1	CapsuleOral	Alembic Pharmaceuticals Limited	46708-085
Fenofibrate	Fenofibrate 200 mg/1	CapsuleOral	Alembic Pharmaceuticals Limited	46708-086
Fenofibrate	Fenofibrate 200 mg/1	CapsuleOral	Alembic Pharmaceuticals Inc.	62332-086
Fenofibrate	Fenofibrate 134 mg/1	CapsuleOral	Alembic Pharmaceuticals Inc.	62332-085