Home – Levothyroxine Sodium
Levothyroxine Sodium
REMEDYREPACK INC.
FULL PRESCRIBING INFORMATION: CONTENTS*
FULL PRESCRIBING INFORMATION
LEVOTHYROXINE SODIUM DESCRIPTION
INACTIVE INGREDIENT
CLINICAL PHARMACOLOGY
PRECAUTIONS
PHARMACOKINETICS
DRUG INTERACTIONS
PREGNANCY
WARNINGS
LEVOTHYROXINE SODIUM CONTRAINDICATIONS
GERIATRIC USE
INFORMATION FOR PATIENTS
LABORATORY TESTS
NURSING MOTHERS
PEDIATRIC USE
LEVOTHYROXINE SODIUM ADVERSE REACTIONS
OVERDOSAGE
HOW SUPPLIED
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Levothyroxine Sodium
Levothyroxine Sodium TABLET
Product Information
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Product Type
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Human prescription drug label |
Item Code (Source)
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NDC:49349-007(NDC:0781-5185) |
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Route of Administration
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ORAL |
DEA Schedule
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Active Ingredient/Active Moiety
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Ingredient Name
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Basis of Strength
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Strength
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LEVOTHYROXINE SODIUM LEVOTHYROXINE |
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0.112 mg
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Product Characteristics
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Color
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Size
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Imprint Code
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Shape
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pink |
9 mm |
112;GG;336 |
CAPSULE |
Packaging
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#
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Item Code
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Package Description
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Marketing Start Date
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Marketing End Date
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1 |
NDC:49349-007-02 |
30 in 1 BLISTER PACK |
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Marketing Information
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Marketing Category
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Application Number or Monograph Citation
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Marketing Start Date
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Marketing End Date
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ANDA |
ANDA076752 |
2010-08-04 |
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PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
