Everolimus

Product NDC
51991-821
11-digit product format
519910821
Labeler code
51991
Product ID
51991-821_fade73fb-a367-4c53-83dd-1352c3ad807b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Everolimus
Dosage form
TABLET
Route
ORAL
Labeler
Breckenridge Pharmaceutical, Inc.
Application
ANDA205426
Marketing category
ANDA
Marketing start
2021-03-05
Substance
EVEROLIMUS
Active strength
2.5 mg/1
Pharmacologic classes
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]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Orange Book products#

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A205426-001EVEROLIMUSEVEROLIMUS2.5MGTABLET / ORALAB2021-03-05
A205426-002EVEROLIMUSEVEROLIMUS5MGTABLET / ORALAB2021-03-05
A205426-003EVEROLIMUSEVEROLIMUS7.5MGTABLET / ORALAB2021-03-05
A205426-004EVEROLIMUSEVEROLIMUS10MGTABLET / ORALAB2021-03-05

Therapeutic equivalence codes#

Application-product, TE code table
Application-productTE code
A205426-001AB
A205426-002AB
A205426-003AB
A205426-004AB

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
EverolimusEVEROLIMUSBreckenridge Pharmaceutical, Inc.01f7b5fb-be0d-4adf-acd2-6899018de9662025-09-05Warnings, Adverse reactionsExact identifier

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

warnings and cautions

5. WARNINGS AND PRECAUTIONS Non-Infectious Pneumonitis: Monitor for clinical symptoms or radiological changes. Withhold or permanently discontinue based on severity. ( 2.9 , 5.1 ) Infections: Monitor for signs and symptoms of infection. Withhold or permanently discontinue based on severity. ( 2.9 , 5.2 ) Severe Hypersensitivity Reactions: Permanently discontinue for clinically significant hypersensitivity. ( 5.3 ) Angioedema: Patients taking concomitant angiotensin-converting-enzyme (ACE) inhibitors may be at increased risk for angioedema. Permanently discontinue for angioedema. ( 5.4 , 7.2 ) Stomatitis: Initiate dexamethasone alcohol-free mouthwash when starting treatment. ( 5.5 , 6.1 ) Renal Failure: Monitor renal function prior to treatment and periodically thereafter. ( 5.6 ) Risk of Impaired Wound Healing: Withhold for at least 1 week prior to elective surgery. Do not administer for at least 2 weeks following major surgery and until adequate wound healing. The safety of resumption of treatment after resolution of wound healing complications has not been established. ( 5.7 ) Geriatric Patients: Monitor and adjust dose for adverse reactions. ( 5.8 ) Metabolic Disorders: Monitor serum glucose and lipids prior to treatment and periodically thereafter. Withhold or permanently discontinue based on severity. ( 2.9 , 5.9 ) Myelosuppression: Monitor hematologic parameters prior to treatment and periodically thereafter. Withhold or permanently discontinue based on severity. ( 2.9 , 5.10 ) Risk of Infection or Reduced Immune Response with Vaccination: Avoid live vaccines and close contact with those who have received live vaccines. Complete recommended childhood vaccinations prior to starting treatment. ( 5.11 ) Radiation Sensitization and Radiation Recall: Severe radiation reactions may occur. ( 5.12 , 6.2 ) Embryo-Fetal Toxicity: Can cause fetal harm. Advise patients of reproductive potential of the potential risk to a fetus and to use effective contraception. ( 5.13 , 8.1 , 8.3 ) 5.1 Non-infectious Pneumonitis Non-infectious pneumonitis is a class effect of rapamycin derivatives. Non-infectious pneumonitis was reported in up to 19% of patients treated with everolimus tablets/everolimus tablets for oral suspension in clinical trials, some cases were reported with pulmonary hypertension (including pulmonary arterial hypertension) as a secondary event. The inci...

Adverse reactions cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

adverse reactions

6. ADVERSE REACTIONS The following serious adverse reactions are described elsewhere in the labeling: Non-Infectious Pneumonitis [see Warnings and Precautions (5.1) ] Infections [see Warnings and Precautions (5.2) ] Severe Hypersensitivity Reactions [see Warnings and Precautions (5.3) ] Angioedema with Concomitant Use of ACE inhibitors [see Warnings and Precautions (5.4) ] Stomatitis [see Warnings and Precautions (5.5) ] Renal Failure [see Warnings and Precautions (5.6) ] Impaired Wound Healing [see Warnings and Precautions (5.7) ] Metabolic Disorders [see Warnings and Precautions (5.9) ] Myelosuppression [see Warnings and Precautions (5.10) ] Radiation Sensitization and Radiation Recall [see Warnings and Precautions (5.12) ] Breast cancer, NET, RCC: Most common adverse reactions (incidence ≥ 30%) include stomatitis, infections, rash, fatigue, diarrhea, edema, abdominal pain, nausea, fever, asthenia, cough, headache, and decreased appetite. ( 6.1 ) TSC-Associated Renal Angiomyolipoma: Most common adverse reaction (incidence ≥ 30%) is stomatitis. ( 6.1 ) TSC-Associated SEGA: Most common adverse reactions (incidence ≥ 30%) are stomatitis and respiratory tract infection. ( 6.1 ) TSC-Associated Partial-Onset Seizures: Most common adverse reaction (incidence ≥ 30%) is stomatitis. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Breckenridge Pharmaceutical, Inc. at 1-800-367-3395 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, the adverse reaction rates observed cannot be directly compared to rates in other trials and may not reflect the rates observed in clinical practice. Hormone Receptor-Positive, HER2-Negative Breast Cancer The safety of everolimus tablets (10 mg orally once daily) in combination with exemestane (25 mg orally once daily) (n = 485) vs. placebo in combination with exemestane (n = 239) was evaluated in a randomized, controlled trial (BOLERO-2) in patients with advanced or metastatic hormone receptor-positive, HER2-negative breast cancer. The median age of patients was 61 years (28 to 93 years), and 75% were White. The median follow-up was approximately 13 months. The most common adverse reactions (incidence ≥ 30%) were stomatitis, infections, rash, fatigue, diarrhea, and decreased appetite. The most common Grade 3-4 adverse reactions (...

adverse reactions table

Table 6: Adverse Reactions Reported in ≥ 10% of Patients With Hormone Receptor-Positive Breast Cancer in BOLERO-2Everolimus Tablets with Exemestane N = 482Placebo with Exemestane N = 238All Grades %Grade 3-4 %All Grades %Grade 3-4 %Grading according to NCI CTCAE Version 3.0.Gastrointestinal StomatitisIncludes stomatitis, mouth ulceration, aphthous stomatitis, glossodynia, gingival pain, glossitis, and lip ulceration.678No Grade 4 adverse reactions were reported.110.8 Diarrhea332180.8 Nausea290.4281 Vomiting171120.8 Constipation140.4130.4 Dry mouth11070General Fatigue364271 Edema peripheral19160.4 Pyrexia150.270.4 Asthenia13240Infections InfectionsIncludes all reported infections, including but not limited to, urinary tract infections, respiratory tract (upper and lower) infections, skin infections, and gastrointestinal tract infections.506252Investigations Weight loss25160Metabolism and nutrition Decreased appetite301120.4 Hyperglycemia14520.4Musculoskeletal and connective tissue Arthralgia200.8170 Back pain140.2100.8 Pain in extremity90.4112Nervous system Dysgeusia220.260 Headache210.4140Psychiatric Insomnia130.280Respiratory, thoracic and mediastinal Cough240.6120 Dyspnea214111 Epistaxis17010 PneumonitisIncludes pneumonitis, interstitial lung disease, lung infiltration, and pulmonary fibrosis.1940.40Skin and subcutaneous tissue Rash39160 Pruritus130.250 Alopecia10050Vascular Hot flush60140

Additional Listing Data#

Finished product
Yes
Brand name base
Everolimus
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
EVEROLIMUS2.5 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9HW64Q8G6G
Rxcui845507, 845515, 998189, 1119400, 1308428, 1308430, 1308432

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
807eb842-6749-6eff-f9ce-2751c69fde93Product name420260122
151279ee-9f3c-b884-3327-05b3fa99d863Product name620251027
a62a50ac-1535-4461-9768-8ae703e2e9fbProduct name120210525
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508
bc07ef78-e82d-0c19-31f4-31f263780582Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51991-821-28Everolimus4 in 1 CARTONTABLET420
51991-821-33Everolimus30 in 1 BOTTLETABLET3020
51991-821-99Everolimus7 in 1 BLISTER PACKTABLET720

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51991-821-28EA - Each51991-821cc60e6ea-fed0-4b1b-b52d-fdfa009919f312021-05-05
51991-821-33EA - Each51991-821c24e7cb2-0e4a-4d62-89f2-8ad0bfe7615512023-07-06
51991-821-99EA - Each51991-82181e82239-dbc4-4ce4-b5a3-9a9e6fd1e8f912021-05-05

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51991-821EVEROLIMUS TABLET EVEROLIMUS TABLET, FOR SUSPENSION [BRECKENRIDGE PHARMACEUTICAL, INC.]16Current NDC, Legacy NDC, 3 package rows20250130_01f7b5fb-be0d-4adf-acd2-6899018de966.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
845507everolimus 10 MG Oral TabletPSN01f7b5fb-be0d-4adf-acd2-6899018de96620
1308428everolimus 2 MG Tablet for Oral SuspensionPSN01f7b5fb-be0d-4adf-acd2-6899018de96620
998189everolimus 2.5 MG Oral TabletPSN01f7b5fb-be0d-4adf-acd2-6899018de96620
1308430everolimus 3 MG Tablet for Oral SuspensionPSN01f7b5fb-be0d-4adf-acd2-6899018de96620
845515everolimus 5 MG Oral TabletPSN01f7b5fb-be0d-4adf-acd2-6899018de96620
1308432everolimus 5 MG Tablet for Oral SuspensionPSN01f7b5fb-be0d-4adf-acd2-6899018de96620
1119400everolimus 7.5 MG Oral TabletPSN01f7b5fb-be0d-4adf-acd2-6899018de96620
845507everolimus 10 MG Oral TabletSCD01f7b5fb-be0d-4adf-acd2-6899018de96620
1308428everolimus 2 MG Tablet for Oral SuspensionSCD01f7b5fb-be0d-4adf-acd2-6899018de96620
998189everolimus 2.5 MG Oral TabletSCD01f7b5fb-be0d-4adf-acd2-6899018de96620
1308430everolimus 3 MG Tablet for Oral SuspensionSCD01f7b5fb-be0d-4adf-acd2-6899018de96620
845515everolimus 5 MG Oral TabletSCD01f7b5fb-be0d-4adf-acd2-6899018de96620
1308432everolimus 5 MG Tablet for Oral SuspensionSCD01f7b5fb-be0d-4adf-acd2-6899018de96620
1119400everolimus 7.5 MG Oral TabletSCD01f7b5fb-be0d-4adf-acd2-6899018de96620

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
51991-821-28519910821284 BLISTER PACK in 1 CARTON (51991-821-28) / 7 TABLET in 1 BLISTER PACK (51991-821-99) 4 blister pack2021-03-050000-00-00NoNoCurrent
51991-821-335199108213330 TABLET in 1 BOTTLE (51991-821-33) 30 tablet2023-06-05NoNoCurrent
51991-821-99519910821997 in 1 BLISTER PACKHistorical