Thyro-Tabs ® Canine (levothyroxine sodium tablets), USP

Manufacturer
MWI/VetOne | LLOYD, Inc. of Iowa
Effective date
2026-10-02
Label type
PRESCRIPTION ANIMAL DRUG LABEL
Version
8
Source
daily-update
Hydrated at
2026-10-07 01:01:43

Label at a glance#

ProductThyro-Tabs Canine
Active ingredientLEVOTHYROXINE SODIUM
Label structure26 sections

Storage and handling

STORAGE CONDITIONS: Store at controlled room temperature 20°-25°C (68°-77°F) with excursions allowed between 15° and 30'C (59° and 86°F). Protect from light and moisture.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Synthetic thyroxine hormone

For oral use in dogs only.

WARNINGS SECTION

CAUTION: Federal (USA) law restricts this drug to use by or on the order of a licensed veterinarian.

DESCRIPTION SECTION

DESCRIPTION: Thyro-Tabs® Canine (levothyroxine sodium tablets), USP contains synthetic crystalline L-3,3' ,5,5'-tetraiodothyronine sodium salt [levothyroxine (T4) sodium]. Synthetic T4 is identical to that produced in the canine thyroid gland. Levothyroxine sodium has an empirical formula of C15H10I4N NaO4 ∙ H2O, molecular weight of 798.85 g/mol (anhydrous), and structural formula as shown:

Chemical Structure
Chemical Structure

VETERINARY INDICATIONS SECTION

INDICATION: For replacement therapy for diminished thyroid function in dogs.

DOSAGE & ADMINISTRATION SECTION

DOSAGE AND ADMINISTRATION: The initial total daily dose is 0.1 mg/10 pounds (0.01 mg/lb; 0.022 mg/kg) body weight as a single dose every 24 hours or as a divided dose every 12 hours.

The dose may then be adjusted by monitoring the serum total thyroxine (TT4) concentrations 4 to 6 hours post-tablet administration, along with clinical response, of the dog every 4 to 8 weeks until an adequate maintenance dose is established.

To minimize day-to-day variations in serum TT4 concentrations (see CLINICAL PHARMACOLOGY), owners should consistently administer Thyro-Tabs Canine either with or without food.

When switching from another levothyroxine sodium formulation to Thyro-Tabs Canine, monitor serum TT4 concentrations and clinical response due to potential differences in recommended starting doses and potential differences in bioavailability.

CONTRAINDICATIONS SECTION

CONTRAINDICATIONS: Do not use in dogs with thyrotoxicosis or uncorrected adrenal insufficiency.

WARNINGS:

WARNINGS SECTION

SPL UNCLASSIFIED SECTION

USER SAFETY WARNINGS: Not for use in humans. Keep out of reach of children. In the event of accidental ingestion, seek medical advice immediately and show the product label to the physician. Wash hands after handling.

SPL UNCLASSIFIED SECTION

ANIMAL SAFETY WARNINGS: Keep Thyro-Tabs Canine in a secure location out of reach of dogs, cats, and other animals to prevent accidental ingestion or overdose.

In humans and rodents, excess in utero exposure to thyroid hormones is associated with hypothalamic-pituitary-thyroid axis dysfunction and morphological thyroid gland defects in the offspring. The safefy of Thyro-Tabs Canine has not been evaluated In breeding, pregnant, or lactating dogs.

PRECAUTIONS SECTION

PRECAUTIONS: Dogs with underlying cardiac disease that are diagnosed with hypothyroidism should be closely monitored during the dose establishment phase. Adjustment of cardiac medication or levothyroxine sodium dosage may be needed depending on clinical response.1-4

ADVERSE REACTIONS:

ADVERSE REACTIONS SECTION

SPL UNCLASSIFIED SECTION

PRE-APPROVAL EXPERIENCE: In a 6-month US field study with 92 dogs, the most commonly reported adverse reactions by percentage of dogs experiencing the reaction included: anorexia (17%), dermatitis (15%), vomiting (15%), otitis externa (14%), lethargy (14%), polydipsia (13%), diarrhea (11 %), leukocytosis (9%), pruritus (8%), tachypnea (8%), polyuria (5%), hyperactivity (4%), and seborrhea (1 %).

One dog was withdrawn from the study at the owner's request because of increased water consumption and urination, which was possibly related to levothyroxine sodium.

Hematocrit and red blood cell counts exceeded the upper limit of the reference range in seven dogs by the end of the study. Liver enzyme (ALP, ALT, or AST) elevations related to levothyroxine administration were reported in three dogs. In two of the dogs with elevated ALT and AST, the elevations resolved by Day 70 and Day 126, respectively.

SPL UNCLASSIFIED SECTION

POST-APPROVAL EXPERIENCE (2022): The following adverse events are based on post-approval adverse drug experience reporting forThyro-Tabs Canine. Not all adverse events are reported to FDA/CVM. It is not always possible to reliably estimate the adverse event frequency or establish a causal relationship to product exposure using these data.

The following adverse events reported in dogs, are listed in decreasing order of reporting frequency: Pruritus, high or low serum thyroxine (T4) concentrations, tachypnea, weight loss, lethargy, anorexia, vomiting, polydipsia, alopecia, dermatitis, hyperactivity, diarrhea, and polyuria.

Allergic-type hypersensitivity reactions (including pruritus, hives, facial swelling, and dermatitis) have also been reported.

SPL UNCLASSIFIED SECTION

CONTACT INFORMATION: To report suspected adverse drug experiences, contact LLOYD, Inc. at 1-800-831-0004 or www.lloydinc.com. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888 FDA-VETS or www.fda.gov/reportanimalae.

CLINICAL PHARMACOLOGY SECTION

CLINICAL PHARMACOLOGY: Levothyroxine sodium has poor oral bioavailability in dogs (10-20%) with peak serum TT4 concentrations wilhin 4 to 6 hours (fasted state). Administration of levothyroxine sodium with food reduces oral bioavailability.5 In most dogs, the estimated half-life is approximately 10-14 hours. Levothyroxine sodium is excreted in the feces.

SPL UNCLASSIFIED SECTION

EFFECTIVENESS: In a US field study with 92 dogs, dogs were administered a starling daily dose of 0.1 mg/10 lb (0.022 mg/kg) body weight. The dose was administered either once every 24 hours or as 0.05 mg/10 lb (0.011 mg/kg) body weight every 12 hours. The dose could be increased or decreased (without a change in frequency) after 6, 10, and 18 weeks, based on clinical findings and serum thyroid hormone concentrations. The maJority of the dogs (80%) were dosed at 0.08-0.12 mg/10 lb (0.008-0.012 mg/lb; 0.018-0.026 mg/kg) by the end of the study, with the majority of dogs (69.7%) requiring one dose change.

The product was considered effective if the serum TT4, free thyroxine (fT4), and thyroid stimulating hormone (TSH) concentrations were all within the desired treatment ranges when collected 4 to 6 hours post-tablet administration after 182 ± 5 days of treatment (TT4: 15-94 nmol/L; fT4: 8-36 pmol/L; TSH: ≤ 37 mU/L). Of the 78 evaluable cases, 59 (75.6%) were considered treatment successes. There was no statistical difference in lhe success rate between the once daily or divided dose treatment groups.

Clinical signs of hypothyroidism (weight gain, lethargy, bradycardia, seborrhea, alopecia, hyperpigmentation, scaling, and hypercholesterolemia) generally improved by the end of the study (Day 182 ± 5). Respiratory rate, excluding panting dogs, increased during the study along with activity level.

SPL UNCLASSIFIED SECTION

TARGET ANIMAL SAFETY: In a laboratory study, levothyroxine sodium was administered to 32 healthy, 7-10 month old, euthyroid Beagle dogs (4 males and 4 females per group) at 0×, 2×, 6×, and 10× the initial dose of 0.10 mg/10 lb (0.01 mg/lb) once daily for 26 weeks. Increased serum TT4 and fT4 concentrations were directly proportional to an increasing dose of levothyroxine sodium. Decreased serum TSH concentrations were inversely proportional to an increasing dose of levothyroxine sodium. Dogs treated with levothyroxine sodium had elevated red blood cell indices (hemoglobin, hematocrit, and red blood cell count) and ALT but these did not exceed the normal reference ranges. Dogs treated with levothyroxine sodium had lower albumin, calcium, globulins, and total protein values but these did not fall below the normal reference ranges. Vomiting, diarrhea, excitation, rapid respiration, tachycardia, and feces with blood were observed in all treatment groups, but were seen with greater frequency in dogs treated with levothyroxine sodium. Decreased pituitary gland and thyroid/parathyroid gland organ weights were also observed in euthyroid dogs treated with levothyroxine sodium.

STORAGE AND HANDLING SECTION

STORAGE CONDITIONS: Store at controlled room temperature 20°-25°C (68°-77°F) with excursions allowed between 15° and 30'C (59° and 86°F). Protect from light and moisture.

HOW SUPPLIED SECTION

HOW SUPPLIED: Thyro-Tabs Canine (levothyroxine sodium tablets), USP is available as scored, color coded ovoid tablets in 9 strengths: 0.1 mg-yellow; 0.2 mg-pink; 0.3 mg-green; 0.4 mg-maroon; 0.5 mg-white; 0.6 mg-purple; 0.7 mg-orange; 0.8 mg-blue; and 1.0 mg-tan, in bottles of 120 and 1,000 tablets.

SPL UNCLASSIFIED SECTION

Approved by FDA under NADA # 141-448

Manufactured by:
LLOYD, Inc.
Shenandoah, IA 51601

Distributed by: MWI
Boise, ID 83705
www.VetOne.net

VET one®

Rev. 07/2026; CIM-03-00

REFERENCES SECTION

REFERENCES:

  1. Phillips DE, Harkin KR. Hypothyroidism and myocardial failure in two Great Danes. J Am Anim Hosp Assoc 2003;39:133-137.
  2. Flood JA, Hoover JP. Improvement in myocardial dysfunction in a hypothyroid dog. Can Vet J 2009;50:828-834.
  3. Chow B, French A. Conversion of atrial fibrillation after levothyroxine in a dog with hypothyroidism and arterial thromboembolism. J Small Anim Pract 2014;55:278-282.
  4. Sangster JK, Panciera DL, Abbott JA. Cardiovascular effects of thyroid disease. Compend Contin Educ Vet 2013;35:E5.
  5. Le Traon G, Burgaud S, Horspool LJ. Pharmacokinetics of total thyroxine in dogs after administration of an oral solution of levothyroxine sodium. J Vet Pharmacol Ther 2008;31:95-101.

SPL UNCLASSIFIED SECTION

For technical questions, call 1-800-831-0004

PRINCIPAL DISPLAY PANEL - 0.1 mg Tablet Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 13985-981-20

VET one®

Thyro-Tabs® Canine
(levothyroxine sodium tablets), USP

0.1 mg

For use in animals only.
Keep out of reach of children.

CAUTION: Federal law restricts this drug to use by
or on the order of a licensed veterinarian.

Approved by FDA under NADA # 141-448

V1 510155
1000 Tablets

PRINCIPAL DISPLAY PANEL - 0.1 mg Tablet Bottle Label
PRINCIPAL DISPLAY PANEL - 0.1 mg Tablet Bottle Label

PRINCIPAL DISPLAY PANEL - 0.2 mg Tablet Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 13985-982-20

VET one®

Thyro-Tabs® Canine
(levothyroxine sodium tablets), USP

0.2 mg

For use in animals only.
Keep out of reach of children.

CAUTION: Federal law restricts this drug to use by
or on the order of a licensed veterinarian.

Approved by FDA under NADA # 141-448

V1 510157
1000 Tablets

PRINCIPAL DISPLAY PANEL - 0.2 mg Tablet Bottle Label
PRINCIPAL DISPLAY PANEL - 0.2 mg Tablet Bottle Label

PRINCIPAL DISPLAY PANEL - 0.3 mg Tablet Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 13985-983-20

VET one®

Thyro-Tabs® Canine
(levothyroxine sodium tablets), USP

0.3 mg

For use in animals only.
Keep out of reach of children.

CAUTION: Federal law restricts this drug to use by
or on the order of a licensed veterinarian.

Approved by FDA under NADA # 141-448

V1 510159
1000 Tablets

PRINCIPAL DISPLAY PANEL - 0.3 mg Tablet Bottle Label
PRINCIPAL DISPLAY PANEL - 0.3 mg Tablet Bottle Label

PRINCIPAL DISPLAY PANEL - 0.4 mg Tablet Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 13985-984-20

VET one®

Thyro-Tabs® Canine
(levothyroxine sodium tablets), USP

0.4 mg

For use in animals only.
Keep out of reach of children.

CAUTION: Federal law restricts this drug to use by
or on the order of a licensed veterinarian.

Approved by FDA under NADA # 141-448

V1 510161
1000 Tablets

PRINCIPAL DISPLAY PANEL - 0.4 mg Tablet Bottle Label
PRINCIPAL DISPLAY PANEL - 0.4 mg Tablet Bottle Label

PRINCIPAL DISPLAY PANEL - 0.5 mg Tablet Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 13985-985-20

VET one®

Thyro-Tabs® Canine
(levothyroxine sodium tablets), USP

0.5 mg

For use in animals only.
Keep out of reach of children.

CAUTION: Federal law restricts this drug to use by
or on the order of a licensed veterinarian.

Approved by FDA under NADA # 141-448

V1 510163
1000 Tablets

PRINCIPAL DISPLAY PANEL - 0.5 mg Tablet Bottle Label
PRINCIPAL DISPLAY PANEL - 0.5 mg Tablet Bottle Label

PRINCIPAL DISPLAY PANEL - 0.6 mg Tablet Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 13985-986-20

VET one®

Thyro-Tabs® Canine
(levothyroxine sodium tablets), USP

0.6 mg

For use in animals only.
Keep out of reach of children.

CAUTION: Federal law restricts this drug to use by
or on the order of a licensed veterinarian.

Approved by FDA under NADA # 141-448

V1 510165
1000 Tablets

PRINCIPAL DISPLAY PANEL - 0.6 mg Tablet Bottle Label
PRINCIPAL DISPLAY PANEL - 0.6 mg Tablet Bottle Label

PRINCIPAL DISPLAY PANEL - 0.7 mg Tablet Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 13985-987-20

VET one®

Thyro-Tabs® Canine
(levothyroxine sodium tablets), USP

0.7 mg

For use in animals only.
Keep out of reach of children.

CAUTION: Federal law restricts this drug to use by
or on the order of a licensed veterinarian.

Approved by FDA under NADA # 141-448

V1 510167
1000 Tablets

PRINCIPAL DISPLAY PANEL - 0.7 mg Tablet Bottle Label
PRINCIPAL DISPLAY PANEL - 0.7 mg Tablet Bottle Label

PRINCIPAL DISPLAY PANEL - 0.8 mg Tablet Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 13985-988-20

VET one®

Thyro-Tabs® Canine
(levothyroxine sodium tablets), USP

0.8 mg

For use in animals only.
Keep out of reach of children.

CAUTION: Federal law restricts this drug to use by
or on the order of a licensed veterinarian.

Approved by FDA under NADA # 141-448

V1 510169
1000 Tablets

PRINCIPAL DISPLAY PANEL - 0.8 mg Tablet Bottle Label
PRINCIPAL DISPLAY PANEL - 0.8 mg Tablet Bottle Label

PRINCIPAL DISPLAY PANEL - 1.0 mg Tablet Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 13985-989-20

VET one®

Thyro-Tabs® Canine
(levothyroxine sodium tablets), USP

1.0 mg

For use in animals only.
Keep out of reach of children.

CAUTION: Federal law restricts this drug to use by
or on the order of a licensed veterinarian.

Approved by FDA under NADA # 141-448

V1 510171
1000 Tablets

PRINCIPAL DISPLAY PANEL - 1.0 mg Tablet Bottle Label
PRINCIPAL DISPLAY PANEL - 1.0 mg Tablet Bottle Label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130313985983207GTIN-13: 0313985983207
EAN-13: 0313985983207
GTIN-12: 313985983207
UPC-A: 313985983207
GTIN storage (14 digits): 00313985983207
thyro-04.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
97c252d3-9bb8-4530-bb44-9824dc7cf556Product name620250729
6c43b71c-35e6-4db3-ba24-c6ef42ff7003Product name320240207
890fd4bf-1a80-42b7-be1b-2d0259d5f0c8Product name520240207
c8ad26bf-af73-460b-b74e-1eff16cc4f9fProduct name520240207
01383843-4069-43cf-aa76-dc17a6f9f8c4Product name220230123
978cca7d-a938-4791-8322-da48d90a63efProduct name120230113
65f86ba3-8816-4e12-899b-18290c8de551Product name220210614
f16ab90f-08c2-40be-a543-66d9827cd1f3Product name120210601
6a33ec05-2ae2-45e5-ab82-2d94b3303923Product name120190709
93355a10-1c44-4c92-a11d-7d995e0200d9Product name120190219

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Older Hydrated Versions#

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VersionEffective dateSourceHydrated
62024-10-17full-release2026-06-01 02:43:39

openFDA label cross-check#

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Matched openFDA labels page 1 of 14 · 272 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Levothyroxine sodiumLEVOTHYROXINE SODIUMREMEDYREPACK INC.bc9385d0-5c67-4bde-94da-e621347e2cba2026-09-10Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM
Levothyroxine sodiumLEVOTHYROXINE SODIUMREMEDYREPACK INC.4c903249-69e9-4168-a9d1-22e6c2c1eb222026-09-10Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM
Levothyroxine sodiumLEVOTHYROXINE SODIUMREMEDYREPACK INC.6f25cbb3-0358-4778-b8f0-f76479a2dcc52026-09-10Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM
Levothyroxine sodiumLEVOTHYROXINE SODIUMREMEDYREPACK INC.7fd988be-ab3d-406d-a55d-1e5a8a2101cc2026-09-10Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM
Levothyroxine sodiumLEVOTHYROXINE SODIUMREMEDYREPACK INC.6108759a-783e-42ca-b078-6a3cd84ce9012026-09-10Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM
Levothyroxine SodiumLEVOTHYROXINE SODIUMREMEDYREPACK INC.13e03769-9a4f-497f-9afa-95bf525090b32026-09-09Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM
LEVOTHYROXINE SODIUMLEVOTHYROXINE SODIUMNorthStar RxLLC58f4dc90-3648-49dc-a7e1-baf918a773b52026-08-20Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM
Levothyroxine SodiumLEVOTHYROXINE SODIUMNuCare Pharmaceuticals, Inc.597ea445-d926-adc6-e063-6394a90a64462026-08-20Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM
Levothyroxine SodiumLEVOTHYROXINE SODIUMCoupler LLC55f4c679-86cb-b97f-e063-6294a90ad5ef2026-07-06Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM
Levothyroxine SodiumLEVOTHYROXINE SODIUMCoupler LLC55f67831-4680-edbf-e063-6294a90a1d362026-07-06Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM
Levothyroxine SodiumLEVOTHYROXINE SODIUMBryant Ranch Prepack489ffba8-983e-478f-8f62-fe08bf3d0e0b2026-06-23Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM
Levothyroxine SodiumLEVOTHYROXINE SODIUMCoupler LLC544d67eb-8487-cb5d-e063-6394a90a31102026-06-15Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM
levothyroxine sodiumLEVOTHYROXINE SODIUMBryant Ranch Prepack3b282e57-1009-4d2c-8ca2-9cca9f7919372026-06-12Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM
Levothyroxine SodiumLEVOTHYROXINE SODIUMCoupler LLC53e84179-fe2a-5696-e063-6394a90a85662026-06-10Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM
LEVOTHYROXINE SODIUMLEVOTHYROXINE SODIUMCoupler LLC5383a4d8-319a-5bf6-e063-6294a90a54972026-06-05Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM
Levothyroxine SodiumLEVOTHYROXINE SODIUMNCS HealthCare of KY, LLC dba Vangard Labsabe173cc-1579-43a5-b12d-a31958d0a5392026-06-04Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM
Levothyroxine SodiumLEVOTHYROXINE SODIUMCardinal Health 107, LLC66a3bd4a-770b-4f67-bfa7-6d5e23f2ecbf2026-06-04Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM
Levothyroxine SodiumLEVOTHYROXINE SODIUMCoupler LLC53316e75-9897-4935-e063-6294a90a94cf2026-06-01Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM
Levothyroxine SodiumLEVOTHYROXINE SODIUMBryant Ranch Prepack5852d874-1ebc-49ff-b6c2-1dd513fca7842026-05-27Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM
Levothyroxine SodiumLEVOTHYROXINE SODIUMA-S Medication Solutionsc8ae9dc4-836f-4912-80d7-684fd374f40a2026-05-27Boxed warning, Warnings, Adverse reactionsName fallback
generic name: LEVOTHYROXINE SODIUM

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.