Clonidine Hydrochloride (Page 3 of 3)

PRINCIPAL DISPLAY PANEL

NDC 52817-180 -10
Clonidine
Hydrochloride
Tablets, USP
0.1 mg
Rx Only 100 Tablets

PRINCIPAL DISPLAY PANEL
NDC 52817-180-10
Clonidine
Hydrochloride
Tablets, USP
0.1 mg
Rx Only
100 Tablets
(click image for full-size original)

PRINCIPAL DISPLAY PANEL

NDC 52817-180 -00
Clonidine
Hydrochloride
Tablets, USP
0.1 mg
Rx Only 1000 Tablets

PRINCIPAL DISPLAY PANEL
NDC 52817-180-00
Clonidine
Hydrochloride
Tablets, USP
0.1 mg
Rx Only
1000 Tablets
(click image for full-size original)

PRINCIPAL DISPLAY PANEL

NDC 52817-18 1 -10
Clonidine
Hydrochloride
Tablets, USP
0.2 mg
Rx Only 100 Tablets

PRINCIPAL DISPLAY PANEL
NDC 52817-181-10
Clonidine
Hydrochloride
Tablets, USP
0.2 mg
Rx Only
100 Tablets
(click image for full-size original)

PRINCIPAL DISPLAY PANEL

NDC 52817-18 1 -00
Clonidine
Hydrochloride
Tablets, USP
0.2 mg
Rx Only 10 0 0 Tablets

PRINCIPAL DISPLAY PANEL
NDC 52817-181-00
Clonidine
Hydrochloride
Tablets, USP
0.2 mg
Rx Only
1000 Tablets
(click image for full-size original)

PRINCIPAL DISPLAY PANEL

NDC 52817-182 -10
Clonidine
Hydrochloride
Tablets, USP
0.3 mg
Rx Only 100 Tablets

PRINCIPAL DISPLAY PANEL
NDC 52817-182-10
Clonidine
Hydrochloride
Tablets, USP
0.3 mg
Rx Only
100 Tablets
(click image for full-size original)

PRINCIPAL DISPLAY PANEL

NDC 52817-182 -00
Clonidine
Hydrochloride
Tablets, USP
0.3 mg
Rx Only 10 0 0 Tablets

PRINCIPAL DISPLAY PANEL
NDC 52817-182-00
Clonidine
Hydrochloride
Tablets, USP
0.3 mg
Rx Only
1000 Tablets
(click image for full-size original)
CLONIDINE HYDROCHLORIDE clonidine hydrochloride tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52817-180
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLONIDINE HYDROCHLORIDE (CLONIDINE) CLONIDINE HYDROCHLORIDE 0.1 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE, UNSPECIFIED FORM
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
STARCH, CORN
SODIUM STARCH GLYCOLATE TYPE A POTATO
D&C YELLOW NO. 10
Product Characteristics
Color YELLOW Score no score
Shape ROUND Size 7mm
Flavor Imprint Code MP;657
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:52817-180-10 100 TABLET in 1 BOTTLE None
2 NDC:52817-180-50 500 TABLET in 1 BOTTLE None
3 NDC:52817-180-00 1000 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA070925 06/01/2017
CLONIDINE HYDROCHLORIDE clonidine hydrochloride tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52817-181
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLONIDINE HYDROCHLORIDE (CLONIDINE) CLONIDINE HYDROCHLORIDE 0.2 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE, UNSPECIFIED FORM
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
STARCH, CORN
SODIUM STARCH GLYCOLATE TYPE A POTATO
Product Characteristics
Color WHITE Score no score
Shape ROUND Size 7mm
Flavor Imprint Code MP;658
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:52817-181-10 100 TABLET in 1 BOTTLE None
2 NDC:52817-181-50 500 TABLET in 1 BOTTLE None
3 NDC:52817-181-00 1000 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA070924 06/01/2017
CLONIDINE HYDROCHLORIDE clonidine hydrochloride tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52817-182
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLONIDINE HYDROCHLORIDE (CLONIDINE) CLONIDINE HYDROCHLORIDE 0.3 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE, UNSPECIFIED FORM
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
STARCH, CORN
SODIUM STARCH GLYCOLATE TYPE A POTATO
D&C YELLOW NO. 10
FD&C BLUE NO. 1
ALUMINUM OXIDE
Product Characteristics
Color GREEN Score no score
Shape ROUND Size 7mm
Flavor Imprint Code MP;659
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:52817-182-10 100 TABLET in 1 BOTTLE None
2 NDC:52817-182-50 500 TABLET in 1 BOTTLE None
3 NDC:52817-182-00 1000 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA070923 06/01/2017
Labeler — TruPharma, LLC (078533947)

Revised: 01/2020 TruPharma, LLC

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