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Adthyza

ADTHYZA™ (thyroid tablets, USP)

Approved
Approval ID

90737b49-1079-46f3-a26e-0119c273b53f

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Feb 23, 2023

Manufacturers
FDA

Azurity Pharmaceuticals, Inc.

DUNS: 117505635

Products 5

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Levothyroxine and Liothyronine

PRODUCT DETAILS

NDC Product Code24338-065
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationORAL
Effective DateFebruary 17, 2023
Generic NameLevothyroxine and Liothyronine

INGREDIENTS (8)

calcium stearateInactive
Code: 776XM7047L
Classification: IACT
LevothyroxineActive
Quantity: 38 ug in 1 1
Code: Q51BO43MG4
Classification: ACTIB
LiothyronineActive
Quantity: 9 ug in 1 1
Code: 06LU7C9H1V
Classification: ACTIB
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
DEXTROSE, UNSPECIFIED FORMInactive
Code: IY9XDZ35W2
Classification: IACT
microcrystalline celluloseInactive
Code: OP1R32D61U
Classification: IACT
mannitolInactive
Code: 3OWL53L36A
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE AInactive
Code: H8AV0SQX4D
Classification: IACT

Levothyroxine and Liothyronine

PRODUCT DETAILS

NDC Product Code24338-032
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationORAL
Effective DateFebruary 17, 2023
Generic NameLevothyroxine and Liothyronine

INGREDIENTS (8)

LevothyroxineActive
Quantity: 19 ug in 1 1
Code: Q51BO43MG4
Classification: ACTIB
calcium stearateInactive
Code: 776XM7047L
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
mannitolInactive
Code: 3OWL53L36A
Classification: IACT
LiothyronineActive
Quantity: 4.5 ug in 1 1
Code: 06LU7C9H1V
Classification: ACTIB
DEXTROSE, UNSPECIFIED FORMInactive
Code: IY9XDZ35W2
Classification: IACT
microcrystalline celluloseInactive
Code: OP1R32D61U
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE AInactive
Code: H8AV0SQX4D
Classification: IACT

Levothyroxine and Liothyronine

PRODUCT DETAILS

NDC Product Code24338-016
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationORAL
Effective DateFebruary 17, 2023
Generic NameLevothyroxine and Liothyronine

INGREDIENTS (8)

calcium stearateInactive
Code: 776XM7047L
Classification: IACT
LevothyroxineActive
Quantity: 9.5 ug in 1 1
Code: Q51BO43MG4
Classification: ACTIB
LiothyronineActive
Quantity: 2.25 ug in 1 1
Code: 06LU7C9H1V
Classification: ACTIB
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
DEXTROSE, UNSPECIFIED FORMInactive
Code: IY9XDZ35W2
Classification: IACT
microcrystalline celluloseInactive
Code: OP1R32D61U
Classification: IACT
mannitolInactive
Code: 3OWL53L36A
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE AInactive
Code: H8AV0SQX4D
Classification: IACT

Levothyroxine and Liothyronine

PRODUCT DETAILS

NDC Product Code24338-113
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationORAL
Effective DateFebruary 17, 2023
Generic NameLevothyroxine and Liothyronine

INGREDIENTS (8)

LiothyronineActive
Quantity: 18 ug in 1 1
Code: 06LU7C9H1V
Classification: ACTIB
calcium stearateInactive
Code: 776XM7047L
Classification: IACT
DEXTROSE, UNSPECIFIED FORMInactive
Code: IY9XDZ35W2
Classification: IACT
LevothyroxineActive
Quantity: 76 ug in 1 1
Code: Q51BO43MG4
Classification: ACTIB
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
microcrystalline celluloseInactive
Code: OP1R32D61U
Classification: IACT
mannitolInactive
Code: 3OWL53L36A
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE AInactive
Code: H8AV0SQX4D
Classification: IACT

Levothyroxine and Liothyronine

PRODUCT DETAILS

NDC Product Code24338-097
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationORAL
Effective DateFebruary 17, 2023
Generic NameLevothyroxine and Liothyronine

INGREDIENTS (8)

LevothyroxineActive
Quantity: 57 ug in 1 1
Code: Q51BO43MG4
Classification: ACTIB
LiothyronineActive
Quantity: 13.5 ug in 1 1
Code: 06LU7C9H1V
Classification: ACTIB
calcium stearateInactive
Code: 776XM7047L
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
DEXTROSE, UNSPECIFIED FORMInactive
Code: IY9XDZ35W2
Classification: IACT
mannitolInactive
Code: 3OWL53L36A
Classification: IACT
microcrystalline celluloseInactive
Code: OP1R32D61U
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE AInactive
Code: H8AV0SQX4D
Classification: IACT

Drug Labeling Information

BOXED WARNING SECTION

LOINC: 34066-1Updated: 2/17/2023

WARNING

ADVERSE REACTIONS SECTION

LOINC: 34084-4Updated: 2/17/2023

ADVERSE REACTIONS

Adverse reactions other than those indicative of hyperthyroidism because of therapeutic overdosage, either initially or during the maintenance period, are rare (See OVERDOSAGE).

DOSAGE & ADMINISTRATION SECTION

LOINC: 34068-7Updated: 2/17/2023

DOSAGE AND ADMINISTRATION

The dosage of thyroid hormones is determined by the indication and must in every case be individualized according to patient response and laboratory findings.

Thyroid hormones are given orally. In acute, emergency conditions, injectable levothyroxine sodium (T4) may be given intravenously when oral administration is not feasible or desirable, as in the treatment of myxedema coma, or during total parenteral nutrition. Intramuscular administration is not advisable because of reported poor absorption.

Hypothyroidism

Therapy is usually instituted using low doses, with increments which depend on the cardiovascular status of the patient. The usual starting dose is 32.5 mg ADTHYZA™ (thyroid tablets, USP), with increments of 16.25 mg every 2 to 3 weeks. A lower starting dosage, 16.25 mg/day, is recommended in patients with long-standing myxedema, particularly if cardiovascular impairment is suspected, in which case extreme caution is recommended. The appearance of angina is an indication for a reduction in dosage. Most patients require 65 to 130 mg/day. Failure to respond to doses of 195 mg suggests lack of compliance or malabsorption. Maintenance dosages 65 to 130 mg/day usually result in normal serum T4 and T3 levels. Adequate therapy usually results in normal TSH and T4 levels after 2 to 3 weeks of therapy.

Readjustment of thyroid hormone dosage should be made within the first four weeks of therapy, after proper clinical and laboratory evaluations, including serum levels of T4, bound and free, and TSH.

Liothyronine (T3) may be used in preference to levothyroxine (T4) during radio-isotope scanning procedures, since induction of hypothyroidism in those cases is more abrupt and can be of shorter duration. It may also be preferred when impairment of peripheral conversion of levothyroxine (T4) and liothyronine (T3) is suspected.

Myxedema Coma

Myxedema coma is usually precipitated in the hypothyroid patient of long- standing by intercurrent illness or drugs such as sedatives and anesthetics and should be considered a medical emergency. Therapy should be directed at the correction of electrolyte disturbances and possible infection besides the administration of thyroid hormones. Corticosteroids should be administered routinely. Levothyroxine (T4) and liothyronine (T3) may be administered via a nasogastric tube but the preferred route of administration of both hormones is intravenous. Levothyroxine sodium (T4) is given at a starting dose of 400 mcg (100 mcg/mL) given rapidly, and is usually well tolerated, even in the elderly. This initial dose is followed by daily supplements of 100 to 200 mcg given IV. Normal T4 levels are achieved in 24 hours followed in 3 days by threefold elevation of T3. Oral therapy with thyroid hormone would be resumed as soon as the clinical situation has been stabilized and the patient is able to take oral medication.

Thyroid Cancer

Exogenous thyroid hormone may produce regression of metastases from follicular and papillary carcinoma of the thyroid and is used as ancillary therapy of these conditions with radioactive iodine. TSH should be suppressed to low or undetectable levels. Therefore, larger amounts of thyroid hormone than those used for replacement therapy are required. Medullary carcinoma of the thyroid is usually unresponsive to this therapy.

Thyroid Suppression Therapy

Administration of thyroid hormone in doses higher than those produced physiologically by the gland results in suppression of the production of endogenous hormone. This is the basis for the thyroid suppression test and is used as an aid in the diagnosis of patients with signs of mild hyperthyroidism in whom base line laboratory tests appear normal, or to demonstrate thyroid gland autonomy in patients with Grave's ophthalmopathy. 131I uptake is determined before and after the administration of the exogenous hormone. A 50% or greater suppression of uptake indicates a normal thyroid-pituitary axis and thus rules out thyroid gland autonomy.

For adults, the usual suppressive dose of levothyroxine (T4) is 1.56 mcg/kg of body weight per day given for 7 to 10 days. These doses usually yield normal serum T4 and T3 levels and lack of response to TSH.

Thyroid hormones should be administered cautiously to patients in whom there is strong suspicion of thyroid gland autonomy, in view of the fact that the exogenous hormone effects will be additive to the endogenous source.

Pediatric Dosage

Pediatric dosage should follow the recommendations summarized in Table 1. In infants with congenital hypothyroidism, therapy with full doses should be instituted as soon as the diagnosis has been made.

Table 1: Recommended Pediatric Dosage for Congenital Hypothyroidism

Age

ADTHYZA™ (thyroid tablets, USP)

Dose per day

Daily dose per kg of body weight

0-6 months

16.25 - 32.5 mg

4.8 - 6 mg

6–12 months

32.5 - 48.75 mg

3.6 - 4.8 mg

1-5 years

48.75 - 65 mg

3 - 3.6 mg

6-12 years

65 - 97.5 mg

2.4 - 3 mg

Over 12 years

Over 97.5 mg

1.2 - 1.8 mg

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Adthyza - FDA Drug Approval Details