Prescription drug · ANDA
Fenofibric acid NDC 68180-129
Choline fenofibrate 135 mg/1 · Capsule, Delayed release · Oral · Lupin Pharmaceuticals, Inc.
NDC codes
FDA NDC DirectoryProduct NDC (as listed)68180-129Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68180-0129Add the package segment from the table below.
Product information
- Brand name (proprietary)
- Fenofibric acid
- Generic name (nonproprietary)
- fenofibric acid
- Active ingredients
- Choline fenofibrate — 135 mg/1
- Dosage form
- Capsule, Delayed release
- Route
- Oral
- Labeler
- Lupin Pharmaceuticals, Inc.
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 200750
- Marketing start
- Listing expires
- Identifiers
- Product ID 68180-129_574221bf-1643-4dd4-8ac6-29f387ce5eafSPL ID 574221bf-1643-4dd4-8ac6-29f387ce5eafSPL set ID b9a3f97c-9e31-4a5f-822f-c9d45e394493RxCUI 828373, 828379UNII 4BMH7IZT98UPC 0368180128014, 0368180129011
- 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.
Product label
Label details couldn’t be retrieved right now. Open the label on DailyMed.