Liothyronine Sodium (Page 5 of 5)

PRINCIPAL DISPLAY PANEL — 25 mcg Tablet Bottle Label

NDC 59762-1207-1
100 Tablets

GREENSTONE® BRAND

liothyroninesodium tablets

25 mcg

Rx only

PRINCIPAL DISPLAY PANEL -- 25 mcg Tablet Bottle Label
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 50 mcg Tablet Bottle Label

NDC 59762-1208-1
100 Tablets

GREENSTONE® BRAND

liothyroninesodium tablets

50 mcg

Rx only

PRINCIPAL DISPLAY PANEL -- 50 mcg Tablet Bottle Label
(click image for full-size original)
LIOTHYRONINE SODIUM liothyronine sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:59762-1206
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LIOTHYRONINE SODIUM (LIOTHYRONINE) LIOTHYRONINE 5 ug
Product Characteristics
Color WHITE (white to off-white) Score no score
Shape ROUND Size 6mm
Flavor Imprint Code KPI;115
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:59762-1206-1 100 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA AUTHORIZED GENERIC NDA010379 02/06/2019
LIOTHYRONINE SODIUM liothyronine sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:59762-1207
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LIOTHYRONINE SODIUM (LIOTHYRONINE) LIOTHYRONINE 25 ug
Product Characteristics
Color WHITE (white to off-white) Score 2 pieces
Shape ROUND Size 7mm
Flavor Imprint Code KPI;116
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:59762-1207-1 100 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA AUTHORIZED GENERIC NDA010379 06/24/2019
LIOTHYRONINE SODIUM liothyronine sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:59762-1208
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LIOTHYRONINE SODIUM (LIOTHYRONINE) LIOTHYRONINE 50 ug
Product Characteristics
Color WHITE (white to off-white) Score 2 pieces
Shape ROUND Size 8mm
Flavor Imprint Code KPI;117
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:59762-1208-1 100 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA AUTHORIZED GENERIC NDA010379 06/24/2019
Labeler — Greenstone LLC (825560733)
Registrant — Pfizer Inc (113480771)
Establishment
Name Address ID/FEI Operations
Peptido GmbH 327335410 API MANUFACTURE (59762-1206), API MANUFACTURE (59762-1207), API MANUFACTURE (59762-1208)

Revised: 11/2020 Greenstone LLC

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