Estradiol (Page 5 of 5)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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ESTRADIOL
estradiol tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68071-2675(NDC:0555-0887)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ESTRADIOL (ESTRADIOL) ESTRADIOL 2 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE
STARCH, CORN
DIBASIC CALCIUM PHOSPHATE DIHYDRATE
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
SODIUM STARCH GLYCOLATE TYPE A POTATO
FD&C BLUE NO. 1 ALUMINUM LAKE
FD&C YELLOW NO. 5
Product Characteristics
Color green Score 2 pieces
Shape OVAL Size 9mm
Flavor Imprint Code 887;2;b
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:68071-2675-9 90 TABLET in 1 BOTTLE None
2 NDC:68071-2675-3 30 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040197 10/28/1997
Labeler — NuCare Pharmaceuticals,Inc. (010632300)
Establishment
Name Address ID/FEI Operations
NuCare Pharmaceuticals,Inc. 010632300 repack (68071-2675)

Revised: 09/2023 NuCare Pharmaceuticals,Inc.

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