NDC Code(s) : 50090-2969-0
Packager : A-S Medication Solutions

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Liothyronine sodiumLiothyronine sodium TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50090-2969(NDC:0378-3611)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LIOTHYRONINE SODIUM(UNII: GCA9VV7D2N)
(LIOTHYRONINE - UNII:06LU7C9H1V) 		LIOTHYRONINE5 ug
Inactive Ingredients
Ingredient Name Strength
CALCIUM SULFATE ANHYDROUS(UNII: E934B3V59H)
GELATIN, UNSPECIFIED(UNII: 2G86QN327L)
STARCH, CORN(UNII: O8232NY3SJ)
STEARIC ACID(UNII: 4ELV7Z65AP)
SUCROSE(UNII: C151H8M554)
TALC(UNII: 7SEV7J4R1U)
Product Characteristics
Color WHITE (white to off-white) Score no score
Shape ROUND Size 6 mm
Flavor Imprint Code ML;11
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:50090-2969-0100 in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product04/10/2017
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090326 10/03/2016

PRINCIPAL DISPLAY PANEL

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