NDC Code(s) : 0054-4179-25, 0054-4180-25, 0054-4181-25, 0054-4182-25, 0054-4182-31, 0054-4183-25, 0054-4184-25, 0054-4186-25, 0054-3176-44, 0054-3177-57, 0054-3177-63, 0054-8179-25, 0054-8180-25, 0054-8174-25, 0054-8181-25, 0054-8176-25, 0054-8175-25, 0054-8183-25
Packager : Hikma Pharmaceuticals USA, Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

DexamethasoneDexamethasone TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0054-4179
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXAMETHASONE(UNII: 7S5I7G3JQL)
(DEXAMETHASONE - UNII:7S5I7G3JQL) 		DEXAMETHASONE0.5 mg
Inactive Ingredients
Ingredient Name Strength
D&C YELLOW NO. 10(UNII: 35SW5USQ3G)
FD&C YELLOW NO. 6(UNII: H77VEI93A8)
LACTOSE MONOHYDRATE(UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE(UNII: 70097M6I30)
STARCH, CORN(UNII: O8232NY3SJ)
SUCROSE(UNII: C151H8M554)
Product Characteristics
Color YELLOW Score 2 pieces
Shape ROUND Size 6 mm
Flavor Imprint Code 54;299
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0054-4179-25100 in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product25/07/1975
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA084611 07/25/1975
DexamethasoneDexamethasone TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0054-4180
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXAMETHASONE(UNII: 7S5I7G3JQL)
(DEXAMETHASONE - UNII:7S5I7G3JQL) 		DEXAMETHASONE0.75 mg
Inactive Ingredients
Ingredient Name Strength
FD&C BLUE NO. 1(UNII: H3R47K3TBD)
LACTOSE MONOHYDRATE(UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE(UNII: 70097M6I30)
STARCH, CORN(UNII: O8232NY3SJ)
SUCROSE(UNII: C151H8M554)
Product Characteristics
Color BLUE (Pale) Score 2 pieces
Shape ROUND (ROUND) Size 6 mm
Flavor Imprint Code 54;960
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0054-4180-25100 in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product06/03/1975
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA084613 06/03/1975
DexamethasoneDexamethasone TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0054-4181
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXAMETHASONE(UNII: 7S5I7G3JQL)
(DEXAMETHASONE - UNII:7S5I7G3JQL) 		DEXAMETHASONE1 mg
Inactive Ingredients
Ingredient Name Strength
FERRIC OXIDE YELLOW(UNII: EX438O2MRT)
LACTOSE MONOHYDRATE(UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE(UNII: 70097M6I30)
STARCH, CORN(UNII: O8232NY3SJ)
SUCROSE(UNII: C151H8M554)
Product Characteristics
Color YELLOW Score 2 pieces
Shape ROUND Size 6 mm
Flavor Imprint Code 54;489
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0054-4181-25100 in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product15/09/1983
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA088306 09/15/1983
DexamethasoneDexamethasone TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0054-4182
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXAMETHASONE(UNII: 7S5I7G3JQL)
(DEXAMETHASONE - UNII:7S5I7G3JQL) 		DEXAMETHASONE1.5 mg
Inactive Ingredients
Ingredient Name Strength
FD&C BLUE NO. 1(UNII: H3R47K3TBD)
FD&C RED NO. 3(UNII: PN2ZH5LOQY)
FD&C RED NO. 40(UNII: WZB9127XOA)
LACTOSE MONOHYDRATE(UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE(UNII: 70097M6I30)
STARCH, CORN(UNII: O8232NY3SJ)
SUCROSE(UNII: C151H8M554)
Product Characteristics
Color PINK Score 2 pieces
Shape ROUND Size 6 mm
Flavor Imprint Code 54;943
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0054-4182-25100 in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product19/05/1975
2NDC:0054-4182-311000 in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product17/07/2006
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA084610 05/19/1975
DexamethasoneDexamethasone TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0054-4183
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXAMETHASONE(UNII: 7S5I7G3JQL)
(DEXAMETHASONE - UNII:7S5I7G3JQL) 		DEXAMETHASONE2 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE(UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE(UNII: 70097M6I30)
STARCH, CORN(UNII: O8232NY3SJ)
SUCROSE(UNII: C151H8M554)
Product Characteristics
Color WHITE Score 2 pieces
Shape ROUND Size 6 mm
Flavor Imprint Code 54;662
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0054-4183-25100 in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product26/08/1982
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA087916 08/26/1982
DexamethasoneDexamethasone TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0054-4184
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXAMETHASONE(UNII: 7S5I7G3JQL)
(DEXAMETHASONE - UNII:7S5I7G3JQL) 		DEXAMETHASONE4 mg
Inactive Ingredients
Ingredient Name Strength
D&C YELLOW NO. 10(UNII: 35SW5USQ3G)
FD&C GREEN NO. 3(UNII: 3P3ONR6O1S)
LACTOSE MONOHYDRATE(UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE(UNII: 70097M6I30)
STARCH, CORN(UNII: O8232NY3SJ)
SUCROSE(UNII: C151H8M554)
FD&C YELLOW NO. 6(UNII: H77VEI93A8)
Product Characteristics
Color GREEN Score 2 pieces
Shape ROUND Size 6 mm
Flavor Imprint Code 54;892
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0054-4184-25100 in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product19/07/1978
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA084612 07/19/1978
DexamethasoneDexamethasone TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0054-4186
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXAMETHASONE(UNII: 7S5I7G3JQL)
(DEXAMETHASONE - UNII:7S5I7G3JQL) 		DEXAMETHASONE6 mg
Inactive Ingredients
Ingredient Name Strength
FD&C GREEN NO. 3(UNII: 3P3ONR6O1S)
LACTOSE MONOHYDRATE(UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE(UNII: 70097M6I30)
STARCH, CORN(UNII: O8232NY3SJ)
SUCROSE(UNII: C151H8M554)
Product Characteristics
Color TURQUOISE (Aqua) Score 2 pieces
Shape ROUND Size 6 mm
Flavor Imprint Code 54;769
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0054-4186-25100 in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product15/09/1983
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA088316 09/15/1983
Dexamethasone IntensolDexamethasone Intensol SOLUTION, CONCENTRATE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0054-3176
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXAMETHASONE(UNII: 7S5I7G3JQL)
(DEXAMETHASONE - UNII:7S5I7G3JQL) 		DEXAMETHASONE1 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
ALCOHOL(UNII: 3K9958V90M)
BENZOIC ACID(UNII: 8SKN0B0MIM)
CITRIC ACID MONOHYDRATE(UNII: 2968PHW8QP)
EDETATE DISODIUM(UNII: 7FLD91C86K)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
WATER(UNII: 059QF0KO0R)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0054-3176-4430 mL in 1 BOTTLE, GLASS Type 1: Convenience Kit of Co-Package09/01/1983
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA088252 09/01/1983
DexamethasoneDexamethasone SOLUTION
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0054-3177
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXAMETHASONE(UNII: 7S5I7G3JQL)
(DEXAMETHASONE - UNII:7S5I7G3JQL) 		DEXAMETHASONE0.5 mg in 5 mL
Inactive Ingredients
Ingredient Name Strength
CITRIC ACID MONOHYDRATE(UNII: 2968PHW8QP)
EDETATE DISODIUM(UNII: 7FLD91C86K)
CHERRY(UNII: BUC5I9595W)
GLYCERIN(UNII: PDC6A3C0OX)
METHYLPARABEN(UNII: A2I8C7HI9T)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
PROPYLPARABEN(UNII: Z8IX2SC1OH)
WATER(UNII: 059QF0KO0R)
SORBITOL(UNII: 506T60A25R)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0054-3177-57240 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product11/01/2007
2NDC:0054-3177-63500 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product09/01/1983
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA088248 09/01/1983
DexamethasoneDexamethasone TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0054-8179
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXAMETHASONE(UNII: 7S5I7G3JQL)
(DEXAMETHASONE - UNII:7S5I7G3JQL) 		DEXAMETHASONE0.5 mg
Inactive Ingredients
Ingredient Name Strength
D&C YELLOW NO. 10(UNII: 35SW5USQ3G)
FD&C YELLOW NO. 6(UNII: H77VEI93A8)
LACTOSE MONOHYDRATE(UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE(UNII: 70097M6I30)
STARCH, CORN(UNII: O8232NY3SJ)
SUCROSE(UNII: C151H8M554)
Product Characteristics
Color YELLOW Score 2 pieces
Shape ROUND Size 6 mm
Flavor Imprint Code 54;299
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0054-8179-2510 in 1 CARTON 25/07/1975
110 in 1 BLISTER PACK Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA084611 07/25/1975
DexamethasoneDexamethasone TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0054-8180
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXAMETHASONE(UNII: 7S5I7G3JQL)
(DEXAMETHASONE - UNII:7S5I7G3JQL) 		DEXAMETHASONE0.75 mg
Inactive Ingredients
Ingredient Name Strength
FD&C BLUE NO. 1(UNII: H3R47K3TBD)
LACTOSE MONOHYDRATE(UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE(UNII: 70097M6I30)
STARCH, CORN(UNII: O8232NY3SJ)
SUCROSE(UNII: C151H8M554)
Product Characteristics
Color BLUE (Pale) Score 2 pieces
Shape ROUND (ROUND) Size 6 mm
Flavor Imprint Code 54;960
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0054-8180-2510 in 1 CARTON 06/03/1975
110 in 1 BLISTER PACK Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA084613 06/03/1975
DexamethasoneDexamethasone TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0054-8174
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXAMETHASONE(UNII: 7S5I7G3JQL)
(DEXAMETHASONE - UNII:7S5I7G3JQL) 		DEXAMETHASONE1 mg
Inactive Ingredients
Ingredient Name Strength
FERRIC OXIDE YELLOW(UNII: EX438O2MRT)
LACTOSE MONOHYDRATE(UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE(UNII: 70097M6I30)
STARCH, CORN(UNII: O8232NY3SJ)
SUCROSE(UNII: C151H8M554)
Product Characteristics
Color YELLOW Score 2 pieces
Shape ROUND Size 6 mm
Flavor Imprint Code 54;489
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0054-8174-2510 in 1 CAN 15/09/1983
110 in 1 BLISTER PACK Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA088306 09/15/1983
DexamethasoneDexamethasone TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0054-8181
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXAMETHASONE(UNII: 7S5I7G3JQL)
(DEXAMETHASONE - UNII:7S5I7G3JQL) 		DEXAMETHASONE1.5 mg
Inactive Ingredients
Ingredient Name Strength
FD&C BLUE NO. 1(UNII: H3R47K3TBD)
FD&C RED NO. 3(UNII: PN2ZH5LOQY)
FD&C RED NO. 40(UNII: WZB9127XOA)
LACTOSE MONOHYDRATE(UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE(UNII: 70097M6I30)
STARCH, CORN(UNII: O8232NY3SJ)
SUCROSE(UNII: C151H8M554)
Product Characteristics
Color PINK Score 2 pieces
Shape ROUND Size 6 mm
Flavor Imprint Code 54;943
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0054-8181-2510 in 1 CARTON 19/05/1975
110 in 1 BLISTER PACK Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA084610 05/19/1975
DexamethasoneDexamethasone TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0054-8176
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXAMETHASONE(UNII: 7S5I7G3JQL)
(DEXAMETHASONE - UNII:7S5I7G3JQL) 		DEXAMETHASONE2 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE(UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE(UNII: 70097M6I30)
STARCH, CORN(UNII: O8232NY3SJ)
SUCROSE(UNII: C151H8M554)
Product Characteristics
Color WHITE Score 2 pieces
Shape ROUND Size 6 mm
Flavor Imprint Code 54;662
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0054-8176-2510 in 1 CARTON 26/08/1982
110 in 1 BLISTER PACK Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA087916 08/26/1982
DexamethasoneDexamethasone TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0054-8175
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXAMETHASONE(UNII: 7S5I7G3JQL)
(DEXAMETHASONE - UNII:7S5I7G3JQL) 		DEXAMETHASONE4 mg
Inactive Ingredients
Ingredient Name Strength
D&C YELLOW NO. 10(UNII: 35SW5USQ3G)
FD&C GREEN NO. 3(UNII: 3P3ONR6O1S)
LACTOSE MONOHYDRATE(UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE(UNII: 70097M6I30)
STARCH, CORN(UNII: O8232NY3SJ)
SUCROSE(UNII: C151H8M554)
FD&C YELLOW NO. 6(UNII: H77VEI93A8)
Product Characteristics
Color GREEN Score 2 pieces
Shape ROUND Size 6 mm
Flavor Imprint Code 54;892
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0054-8175-2510 in 1 CARTON 19/07/1978
110 in 1 BLISTER PACK Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA084612 07/19/1978
DexamethasoneDexamethasone TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0054-8183
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXAMETHASONE(UNII: 7S5I7G3JQL)
(DEXAMETHASONE - UNII:7S5I7G3JQL) 		DEXAMETHASONE6 mg
Inactive Ingredients
Ingredient Name Strength
FD&C GREEN NO. 3(UNII: 3P3ONR6O1S)
LACTOSE MONOHYDRATE(UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE(UNII: 70097M6I30)
STARCH, CORN(UNII: O8232NY3SJ)
SUCROSE(UNII: C151H8M554)
Product Characteristics
Color TURQUOISE (Aqua) Score 2 pieces
Shape ROUND Size 6 mm
Flavor Imprint Code 54;769
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0054-8183-2510 in 1 CARTON 15/09/1983
110 in 1 BLISTER PACK Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA088316 09/15/1983

LABELER - Hikma Pharmaceuticals USA, Inc.(080189610)

Establishment
Name Address ID/FEI Business Operations
West-Ward Columbus Inc. 058839929 MANUFACTURE(0054-4179, 0054-4180, 0054-4181, 0054-4182, 0054-4183, 0054-4184, 0054-4186, 0054-3176, 0054-3177, 0054-8179, 0054-8180, 0054-8174, 0054-8181, 0054-8176, 0054-8175, 0054-8183)

PRINCIPAL DISPLAY PANEL

NDC 0054-4179-25     100 Tablets
Dexamethasone Tablets, USP
0.5 mg

0.5 mg Bottle Label

PRINCIPAL DISPLAY PANEL

NDC 0054-8179-25     10x10 Unit-Dose Tablets
Dexamethasone Tablets, USP
0.5 mg

0.5 mg Unit-Dose Carton

PRINCIPAL DISPLAY PANEL

NDC 0054-4180-25     100 Tablets
Dexamethasone Tablets, USP
0.75 mg

0.75 mg Bottle Label

PRINCIPAL DISPLAY PANEL

NDC 0054-8180-25     10x10 Unit-Dose Tablets
Dexamethasone Tablets, USP
0.75 mg

0.75 Unit-Dose Carton

PRINCIPAL DISPLAY PANEL

NDC 0054-4181-25     100 Tablets
Dexamethasone Tablets, USP
1 mg

1 mg Bottle Label

PRINCIPAL DISPLAY PANEL

NDC 0054-8174-25     10x10 Unit-Dose Tablets
Dexamethasone Tablets, USP
1 mg

1 mg Unit-Dose Carton

PRINCIPAL DISPLAY PANEL

NDC 0054-4182-25     100 Tablets
Dexamethasone Tablets, USP
1.5 mg

1.5 mg Bottle Label

PRINCIPAL DISPLAY PANEL

NDC 0054-8181-25     10x10 Unit-Dose Tablets
Dexamethasone Tablets, USP
1.5 mg

1.5 mg Unit-Dose Carton

PRINCIPAL DISPLAY PANEL

NDC 0054-4183-25     100 Tablets
Dexamethasone Tablets, USP
2 mg

2 mg Bottle Label

PRINCIPAL DISPLAY PANEL

NDC 0054-8176-25     10x10 Unit-Dose Tablets
Dexamethasone Tablets, USP
2 mg

2 mg Unit-Dose Carton

PRINCIPAL DISPLAY PANEL

NDC 0054-4184-25     100 Tablets
Dexamethasone Tablets, USP
4 mg

4 mg Bottle Label

PRINCIPAL DISPLAY PANEL

NDC 0054-8175-25     10x10 Unit-Dose Tablets
Dexamethasone Tablets, USP
4 mg

4 mg Unit-Dose Carton

PRINCIPAL DISPLAY PANEL

NDC 0054-4186-25     100 Tablets
Dexamethasone Tablets, USP
6 mg

6 mg Bottle Label

PRINCIPAL DISPLAY PANEL

NDC 0054-8183-25     10x10 Unit-Dose Tablets
Dexamethasone Tablets, USP
6 mg

6 mg Unit-Dose Carton

PRINCIPAL DISPLAY PANEL

NDC 0054-3177-57     240 mL
Dexamethasone Oral Solution, USP
0.5 mg per 5 mL

0.5 mg per 5 mL Oral Solution Bottle Label

PRINCIPAL DISPLAY PANEL

NDC 0054-3176-44     30 mL
Dexamethasone Oral Solution, USP
Intensol™ (Concentrate)
1 mg per mL

1 mg per mL Intensol Oral Solution