everolimus

Generic: everolimus

Labeler: ascend laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name everolimus
Generic Name everolimus
Labeler ascend laboratories, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

everolimus .5 mg/1

Manufacturer
Ascend Laboratories, LLC

Identifiers & Regulatory

Product NDC 67877-719
Product ID 67877-719_33247fe5-9b47-4513-93fe-fc65e4c1b63f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214138
Listing Expiration 2026-12-31
Marketing Start 2021-11-27

Pharmacologic Class

Established (EPC)
kinase inhibitor [epc] mtor inhibitor immunosuppressant [epc]
Mechanism of Action
protein kinase inhibitors [moa] cytochrome p450 3a4 inhibitors [moa] cytochrome p450 2d6 inhibitors [moa] mtor inhibitors [moa]
Physiologic Effect
decreased immunologic activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67877719
Hyphenated Format 67877-719

Supplemental Identifiers

RxCUI
977427 977434 977438 2056895
UPC
0367877721316 0367877720319 0367877719313 0367877718316
UNII
9HW64Q8G6G
NUI
N0000175605 N0000175076 N0000182141 N0000182137 N0000175625 N0000175624 N0000175550

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 everolimus (source: ndc)
Generic Name everolimus (source: ndc)
Application Number ANDA214138 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/1
source: ndc
Packaging
  • 6 BLISTER PACK in 1 CARTON (67877-719-31) / 10 TABLET in 1 BLISTER PACK (67877-719-33)
  • 60 TABLET in 1 BOTTLE (67877-719-60)
source: ndc

Packages (2)

67877-719-31 6 BLISTER PACK in 1 CARTON (67877-719-31) / 10 TABLET in 1 BLISTER PACK (67877-719-33) 67877-719-60 60 TABLET in 1 BOTTLE (67877-719-60)

Ingredients (1)

everolimus (.5 mg/1)

Linked Drug Pages (1)

Everolimus ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "33247fe5-9b47-4513-93fe-fc65e4c1b63f", "openfda": {"nui": ["N0000175605", "N0000175076", "N0000182141", "N0000182137", "N0000175625", "N0000175624", "N0000175550"], "upc": ["0367877721316", "0367877720319", "0367877719313", "0367877718316"], "unii": ["9HW64Q8G6G"], "rxcui": ["977427", "977434", "977438", "2056895"], "spl_set_id": ["2693c497-a70b-4d00-b6db-602c872e5bed"], "pharm_class_pe": ["Decreased Immunologic Activity [PE]"], "pharm_class_epc": ["Kinase Inhibitor [EPC]", "mTOR Inhibitor Immunosuppressant [EPC]"], "pharm_class_moa": ["Protein Kinase Inhibitors [MoA]", "Cytochrome P450 3A4 Inhibitors [MoA]", "Cytochrome P450 2D6 Inhibitors [MoA]", "mTOR Inhibitors [MoA]"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 BLISTER PACK in 1 CARTON (67877-719-31)  / 10 TABLET in 1 BLISTER PACK (67877-719-33)", "package_ndc": "67877-719-31", "marketing_start_date": "20211127"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (67877-719-60)", "package_ndc": "67877-719-60", "marketing_start_date": "20240301"}], "brand_name": "Everolimus", "product_id": "67877-719_33247fe5-9b47-4513-93fe-fc65e4c1b63f", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Cytochrome P450 3A4 Inhibitors [MoA]", "Decreased Immunologic Activity [PE]", "Kinase Inhibitor [EPC]", "Protein Kinase Inhibitors [MoA]", "mTOR Inhibitor Immunosuppressant [EPC]", "mTOR Inhibitors [MoA]"], "product_ndc": "67877-719", "generic_name": "Everolimus", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Everolimus", "active_ingredients": [{"name": "EVEROLIMUS", "strength": ".5 mg/1"}], "application_number": "ANDA214138", "marketing_category": "ANDA", "marketing_start_date": "20211127", "listing_expiration_date": "20261231"}