fenofibric acid

Generic: fenofibric acid

Labeler: alembic pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fenofibric acid
Generic Name fenofibric acid
Labeler alembic pharmaceuticals inc.
Dosage Form CAPSULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

fenofibric acid 45 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-244
Product ID 62332-244_fdb85004-0a66-487a-992c-61764da679b4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208705
Listing Expiration 2026-12-31
Marketing Start 2017-05-15

Pharmacologic Class

Established (EPC)
peroxisome proliferator receptor alpha agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62332244
Hyphenated Format 62332-244

Supplemental Identifiers

RxCUI
828373 828379
UNII
BGF9MN2HU1
NUI
N0000175596

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name fenofibric acid (source: ndc)
Generic Name fenofibric acid (source: ndc)
Application Number ANDA208705 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 45 mg/1
source: ndc
Packaging
  • 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-244-30)
  • 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-244-90)
  • 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-244-91)
source: ndc

Packages (3)

62332-244-30 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-244-30) 62332-244-90 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-244-90) 62332-244-91 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-244-91)

Ingredients (1)

fenofibric acid (45 mg/1)

Linked Drug Pages (1)

Fenofibric Acid ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fdb85004-0a66-487a-992c-61764da679b4", "openfda": {"nui": ["N0000175596"], "unii": ["BGF9MN2HU1"], "rxcui": ["828373", "828379"], "spl_set_id": ["8ffcb173-095a-4550-84f2-18959ad2aab8"], "pharm_class_epc": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-244-30)", "package_ndc": "62332-244-30", "marketing_start_date": "20170515"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-244-90)", "package_ndc": "62332-244-90", "marketing_start_date": "20170515"}, {"sample": false, "description": "1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-244-91)", "package_ndc": "62332-244-91", "marketing_start_date": "20170515"}], "brand_name": "Fenofibric Acid", "product_id": "62332-244_fdb85004-0a66-487a-992c-61764da679b4", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "62332-244", "generic_name": "Fenofibric Acid", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fenofibric Acid", "active_ingredients": [{"name": "FENOFIBRIC ACID", "strength": "45 mg/1"}], "application_number": "ANDA208705", "marketing_category": "ANDA", "marketing_start_date": "20170515", "listing_expiration_date": "20261231"}