NDC Code(s) : 55700-056-28, 55700-056-30, 55700-056-60
Packager : Lake Erie Medical DBA Quality Care Products LLC

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:55700-056(NDC:42794-019)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LIOTHYRONINE SODIUM(UNII: GCA9VV7D2N)
(LIOTHYRONINE - UNII:06LU7C9H1V) 		LIOTHYRONINE25 ug
Inactive Ingredients
Ingredient Name Strength
CALCIUM SULFATE DIHYDRATE(UNII: 4846Q921YM)
STARCH, CORN(UNII: O8232NY3SJ)
GELATIN(UNII: 2G86QN327L)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MANNITOL(UNII: 3OWL53L36A)
Product Characteristics
Color white Score 2
Shape ROUND Size 7 mm
Flavor Imprint Code 19
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:55700-056-2828 in 1 BOTTLE Type 0: Not a Combination Product30/11/2012
2NDC:55700-056-3030 in 1 BOTTLE Type 0: Not a Combination Product30/11/2012
3NDC:55700-056-6060 in 1 BOTTLE Type 0: Not a Combination Product30/11/2012
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA200295 11/30/2012

PRINCIPAL DISPLAY PANEL

Image of Label