Levothyroxine Sodium Anhydrous

CHEBI:CHEBI_748078

Drug Classification

Important Medical Information

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Additional Identifiers

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Additional Attributes

rxcui
1115269
product_type
HUMAN PRESCRIPTION DRUG
marketing_category
ANDA
listing_expiration_date
20241231
brand_name
Levothyroxine Sodium
brand_name_base
Levothyroxine Sodium
pharm_class
l-Thyroxine [EPC]
route
INTRAVENOUS
dosage_form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
marketing_start_date
20181227
package_marketing_start_date
20181227
labeler_name
MAIA Pharmaceuticals, Inc.
manufacturer_name
MAIA Pharmaceuticals, Inc.
generic_name
LEVOTHYROXINE SODIUM ANHYDROUS
product_ndc
42023-202
application_number
NDA202231
spl_id
c2f1de80-e517-401f-9ef4-006545f79f9f
active_ingredient_name
LEVOTHYROXINE SODIUM ANHYDROUS
active_ingredient_strength
100 ug/5mL
package_ndc
42023-202-01
package_description
1 VIAL, SINGLE-DOSE in 1 CARTON (42023-202-01) / 5 mL in 1 VIAL, SINGLE-DOSE
unii
054I36CPMN
spl_set_id
f88f44d8-2f18-4155-9d78-6323d19fbafe
22-rdf-syntax-ns#type
http://www.w3.org/2002/07/owl#Class