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.
Other NDCs under ANDA 200750
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Fenofibric acid | Choline fenofibrate 45 mg/1 | Capsule, Delayed releaseOral | Lupin Pharmaceuticals, Inc. | 68180-128 |