Diazepam (Page 4 of 4)

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DIAZEPAM
diazepam tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53217-184(NDC:0172-3926)
Route of Administration ORAL DEA Schedule CIV
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DIAZEPAM (DIAZEPAM) DIAZEPAM 5 mg
Inactive Ingredients
Ingredient Name Strength
ANHYDROUS LACTOSE
SILICON DIOXIDE
D&C YELLOW NO. 10
ALUMINUM OXIDE
FD&C YELLOW NO. 6
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
STARCH, CORN
SODIUM STARCH GLYCOLATE TYPE A POTATO
Product Characteristics
Color YELLOW Score 2 pieces
Shape ROUND Size 8mm
Flavor Imprint Code 3926;TEVA
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53217-184-00 100 TABLET in 1 BOTTLE None
2 NDC:53217-184-02 120 TABLET in 1 BOTTLE None
3 NDC:53217-184-05 5 TABLET in 1 BOTTLE None
4 NDC:53217-184-07 7 TABLET in 1 BOTTLE None
5 NDC:53217-184-08 8 TABLET in 1 BOTTLE None
6 NDC:53217-184-10 10 TABLET in 1 BOTTLE None
7 NDC:53217-184-14 14 TABLET in 1 BOTTLE None
8 NDC:53217-184-20 20 TABLET in 1 BOTTLE None
9 NDC:53217-184-29 2 TABLET in 1 BOTTLE None
10 NDC:53217-184-30 30 TABLET in 1 BOTTLE None
11 NDC:53217-184-31 3 TABLET in 1 BOTTLE None
12 NDC:53217-184-60 60 TABLET in 1 BOTTLE None
13 NDC:53217-184-90 90 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA071321 12/10/1986
DIAZEPAM
diazepam tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53217-185(NDC:0172-3927)
Route of Administration ORAL DEA Schedule CIV
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DIAZEPAM (DIAZEPAM) DIAZEPAM 10 mg
Inactive Ingredients
Ingredient Name Strength
ANHYDROUS LACTOSE
SILICON DIOXIDE
FD&C BLUE NO. 1
ALUMINUM OXIDE
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
STARCH, CORN
SODIUM STARCH GLYCOLATE TYPE A POTATO
Product Characteristics
Color BLUE (light blue) Score 2 pieces
Shape ROUND Size 8mm
Flavor Imprint Code 3927;TEVA
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53217-185-00 100 TABLET in 1 BOTTLE None
2 NDC:53217-185-02 120 TABLET in 1 BOTTLE None
3 NDC:53217-185-05 5 TABLET in 1 BOTTLE None
4 NDC:53217-185-07 7 TABLET in 1 BOTTLE None
5 NDC:53217-185-08 8 TABLET in 1 BOTTLE None
6 NDC:53217-185-10 10 TABLET in 1 BOTTLE None
7 NDC:53217-185-14 14 TABLET in 1 BOTTLE None
8 NDC:53217-185-20 20 TABLET in 1 BOTTLE None
9 NDC:53217-185-29 2 TABLET in 1 BOTTLE None
10 NDC:53217-185-30 30 TABLET in 1 BOTTLE None
11 NDC:53217-185-31 3 TABLET in 1 BOTTLE None
12 NDC:53217-185-60 60 TABLET in 1 BOTTLE None
13 NDC:53217-185-90 90 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA071322 12/10/1986
Labeler — Aidarex Pharmaceuticals LLC (801503249)

Revised: 03/2017 Aidarex Pharmaceuticals LLC

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