Memantine Hydrochloride (Page 5 of 5)

Principal Display Panel

NDC 59115-172-60
Memantine Hydrochloride
Tablets, USP
5 mg
Rx Only60 Tablets

NDC 59115-172-60
Memantine Hydrochloride
Tablets, USP
5 mg
Rx Only
60 Tablets
(click image for full-size original)

Principal Display Panel

NDC 59115-173-60
Memantine Hydrochloride
Tablets, USP
10 mg
Rx Only60 Tablets

NDC 59115-173-60
Memantine Hydrochloride
Tablets, USP
10 mg
Rx Only
60 Tablets
(click image for full-size original)
MEMANTINE HYDROCHLORIDE memantine hydrochloride tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:59115-172
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MEMANTINE HYDROCHLORIDE (MEMANTINE) MEMANTINE HYDROCHLORIDE 5 mg
Inactive Ingredients
Ingredient Name Strength
CELLULOSE, MICROCRYSTALLINE
SILICON DIOXIDE
CROSCARMELLOSE SODIUM
TALC
MAGNESIUM STEARATE
HYPROMELLOSES
TITANIUM DIOXIDE
POLYSORBATE 80
FD&C YELLOW NO. 6
FD&C BLUE NO. 2
Product Characteristics
Color ORANGE Score no score
Shape CAPSULE Size 9mm
Flavor Imprint Code W121
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:59115-172-60 60 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA208173 01/23/2020
MEMANTINE HYDROCHLORIDE memantine hydrochloride tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:59115-173
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MEMANTINE HYDROCHLORIDE (MEMANTINE) MEMANTINE HYDROCHLORIDE 10 mg
Inactive Ingredients
Ingredient Name Strength
CELLULOSE, MICROCRYSTALLINE
SILICON DIOXIDE
CROSCARMELLOSE SODIUM
TALC
MAGNESIUM STEARATE
HYPROMELLOSES
TITANIUM DIOXIDE
POLYSORBATE 80
FERROSOFERRIC OXIDE
Product Characteristics
Color GRAY Score no score
Shape CAPSULE Size 11mm
Flavor Imprint Code W122
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:59115-173-60 60 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA208173 01/23/2020
Labeler — Hikma Pharmaceutical (534661645)

Revised: 05/2016 Hikma Pharmaceutical

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