NDC Code(s) : 57664-047-88, 57664-046-88, 57664-048-88, 57664-049-88, 57664-050-88, 57664-051-88, 57664-052-88, 57664-083-88, 57664-084-88, 57664-085-88, 57664-086-88, 57664-087-88, 57664-088-88
Packager : Sun Pharmaceutical Industries, Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : CII

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

LISDEXAMFETAMINE DIMESYLATELISDEXAMFETAMINE DIMESYLATE CAPSULE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57664-047
Route of Administration ORAL DEA Schedule CII
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LISDEXAMFETAMINE DIMESYLATE(UNII: SJT761GEGS)
(LISDEXAMFETAMINE - UNII:H645GUL8KJ) 		LISDEXAMFETAMINE DIMESYLATE20 mg
Inactive Ingredients
Ingredient Name Strength
FERRIC OXIDE YELLOW(UNII: EX438O2MRT)
FERROSOFERRIC OXIDE(UNII: XM0M87F357)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
GELATIN, UNSPECIFIED(UNII: 2G86QN327L)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
SHELLAC(UNII: 46N107B71O)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
Product Characteristics
Color white (white to off-white opaque) Score no score
Shape CAPSULE Size 16 mm
Flavor Imprint Code RM47;20mg
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:57664-047-88100 in 1 BOTTLE Type 0: Not a Combination Product25/08/2023
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA214484 08/25/2023
LISDEXAMFETAMINE DIMESYLATELISDEXAMFETAMINE DIMESYLATE CAPSULE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57664-046
Route of Administration ORAL DEA Schedule CII
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LISDEXAMFETAMINE DIMESYLATE(UNII: SJT761GEGS)
(LISDEXAMFETAMINE - UNII:H645GUL8KJ) 		LISDEXAMFETAMINE DIMESYLATE10 mg
Inactive Ingredients
Ingredient Name Strength
FERROSOFERRIC OXIDE(UNII: XM0M87F357)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
GELATIN, UNSPECIFIED(UNII: 2G86QN327L)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
SHELLAC(UNII: 46N107B71O)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
FD&C RED NO. 3(UNII: PN2ZH5LOQY)
Product Characteristics
Color pink (pink opaque) Score no score
Shape CAPSULE Size 14 mm
Flavor Imprint Code RM46;10mg
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:57664-046-88100 in 1 BOTTLE Type 0: Not a Combination Product25/08/2023
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA214484 08/25/2023
LISDEXAMFETAMINE DIMESYLATELISDEXAMFETAMINE DIMESYLATE CAPSULE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57664-048
Route of Administration ORAL DEA Schedule CII
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LISDEXAMFETAMINE DIMESYLATE(UNII: SJT761GEGS)
(LISDEXAMFETAMINE - UNII:H645GUL8KJ) 		LISDEXAMFETAMINE DIMESYLATE30 mg
Inactive Ingredients
Ingredient Name Strength
FERROSOFERRIC OXIDE(UNII: XM0M87F357)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
GELATIN, UNSPECIFIED(UNII: 2G86QN327L)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
SHELLAC(UNII: 46N107B71O)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
D&C RED NO. 28(UNII: 767IP0Y5NH)
FD&C RED NO. 40(UNII: WZB9127XOA)
FD&C YELLOW NO. 6(UNII: H77VEI93A8)
Product Characteristics
Color orange (orange opaque), white (white opaque) Score no score
Shape CAPSULE Size 16 mm
Flavor Imprint Code RM48;30mg
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:57664-048-88100 in 1 BOTTLE Type 0: Not a Combination Product25/08/2023
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA214484 08/25/2023
LISDEXAMFETAMINE DIMESYLATELISDEXAMFETAMINE DIMESYLATE CAPSULE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57664-049
Route of Administration ORAL DEA Schedule CII
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LISDEXAMFETAMINE DIMESYLATE(UNII: SJT761GEGS)
(LISDEXAMFETAMINE - UNII:H645GUL8KJ) 		LISDEXAMFETAMINE DIMESYLATE40 mg
Inactive Ingredients
Ingredient Name Strength
FERROSOFERRIC OXIDE(UNII: XM0M87F357)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
GELATIN, UNSPECIFIED(UNII: 2G86QN327L)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
SHELLAC(UNII: 46N107B71O)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
FD&C BLUE NO. 1(UNII: H3R47K3TBD)
FERRIC OXIDE YELLOW(UNII: EX438O2MRT)
Product Characteristics
Color green (dark green opaque), white (white opaque) Score no score
Shape CAPSULE Size 16 mm
Flavor Imprint Code RM49;40mg
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:57664-049-88100 in 1 BOTTLE Type 0: Not a Combination Product25/08/2023
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA214484 08/25/2023
LISDEXAMFETAMINE DIMESYLATELISDEXAMFETAMINE DIMESYLATE CAPSULE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57664-050
Route of Administration ORAL DEA Schedule CII
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LISDEXAMFETAMINE DIMESYLATE(UNII: SJT761GEGS)
(LISDEXAMFETAMINE - UNII:H645GUL8KJ) 		LISDEXAMFETAMINE DIMESYLATE50 mg
Inactive Ingredients
Ingredient Name Strength
FERROSOFERRIC OXIDE(UNII: XM0M87F357)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
GELATIN, UNSPECIFIED(UNII: 2G86QN327L)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
SHELLAC(UNII: 46N107B71O)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
D&C RED NO. 28(UNII: 767IP0Y5NH)
FD&C BLUE NO. 1(UNII: H3R47K3TBD)
Product Characteristics
Color blue (blue opaque), white (white opaque) Score no score
Shape CAPSULE Size 16 mm
Flavor Imprint Code RM50;50mg
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:57664-050-88100 in 1 BOTTLE Type 0: Not a Combination Product25/08/2023
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA214484 08/25/2023
LISDEXAMFETAMINE DIMESYLATELISDEXAMFETAMINE DIMESYLATE CAPSULE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57664-051
Route of Administration ORAL DEA Schedule CII
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LISDEXAMFETAMINE DIMESYLATE(UNII: SJT761GEGS)
(LISDEXAMFETAMINE - UNII:H645GUL8KJ) 		LISDEXAMFETAMINE DIMESYLATE60 mg
Inactive Ingredients
Ingredient Name Strength
FERROSOFERRIC OXIDE(UNII: XM0M87F357)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
GELATIN, UNSPECIFIED(UNII: 2G86QN327L)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
SHELLAC(UNII: 46N107B71O)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
FD&C BLUE NO. 1(UNII: H3R47K3TBD)
Product Characteristics
Color blue (aqua blue opaque) Score no score
Shape CAPSULE Size 18 mm
Flavor Imprint Code RM51;60mg
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:57664-051-88100 in 1 BOTTLE Type 0: Not a Combination Product25/08/2023
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA214484 08/25/2023
LISDEXAMFETAMINE DIMESYLATELISDEXAMFETAMINE DIMESYLATE CAPSULE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57664-052
Route of Administration ORAL DEA Schedule CII
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LISDEXAMFETAMINE DIMESYLATE(UNII: SJT761GEGS)
(LISDEXAMFETAMINE - UNII:H645GUL8KJ) 		LISDEXAMFETAMINE DIMESYLATE70 mg
Inactive Ingredients
Ingredient Name Strength
FERROSOFERRIC OXIDE(UNII: XM0M87F357)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
GELATIN, UNSPECIFIED(UNII: 2G86QN327L)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
SHELLAC(UNII: 46N107B71O)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
D&C RED NO. 28(UNII: 767IP0Y5NH)
FD&C RED NO. 40(UNII: WZB9127XOA)
FD&C YELLOW NO. 6(UNII: H77VEI93A8)
FD&C BLUE NO. 1(UNII: H3R47K3TBD)
Product Characteristics
Color blue (blue opaque), orange (orange opaque) Score no score
Shape CAPSULE Size 18 mm
Flavor Imprint Code RM52;70mg
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:57664-052-88100 in 1 BOTTLE Type 0: Not a Combination Product25/08/2023
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA214484 08/25/2023
LISDEXAMFETAMINE DIMESYLATELISDEXAMFETAMINE DIMESYLATE TABLET, CHEWABLE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57664-083
Route of Administration ORAL DEA Schedule CII
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LISDEXAMFETAMINE DIMESYLATE(UNII: SJT761GEGS)
(LISDEXAMFETAMINE - UNII:H645GUL8KJ) 		LISDEXAMFETAMINE DIMESYLATE10 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
MALTODEXTRIN(UNII: 7CVR7L4A2D)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
GUAR GUM(UNII: E89I1637KE)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MANNITOL(UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE)(UNII: 461P5CJN6T)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
SUCRALOSE(UNII: 96K6UQ3ZD4)
Product Characteristics
Color white (White to off white) Score no score
Shape ROUND Size 7 mm
Flavor STRAWBERRY Imprint Code 10;S83
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:57664-083-88100 in 1 BOTTLE Type 0: Not a Combination Product25/08/2023
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA214134 08/25/2023
LISDEXAMFETAMINE DIMESYLATELISDEXAMFETAMINE DIMESYLATE TABLET, CHEWABLE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57664-084
Route of Administration ORAL DEA Schedule CII
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LISDEXAMFETAMINE DIMESYLATE(UNII: SJT761GEGS)
(LISDEXAMFETAMINE - UNII:H645GUL8KJ) 		LISDEXAMFETAMINE DIMESYLATE20 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
MALTODEXTRIN(UNII: 7CVR7L4A2D)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
GUAR GUM(UNII: E89I1637KE)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MANNITOL(UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE)(UNII: 461P5CJN6T)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
SUCRALOSE(UNII: 96K6UQ3ZD4)
Product Characteristics
Color white (White to off white) Score no score
Shape HEXAGON (6 sided) Size 10 mm
Flavor STRAWBERRY Imprint Code 20;S84
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:57664-084-88100 in 1 BOTTLE Type 0: Not a Combination Product25/08/2023
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA214134 08/25/2023
LISDEXAMFETAMINE DIMESYLATELISDEXAMFETAMINE DIMESYLATE TABLET, CHEWABLE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57664-085
Route of Administration ORAL DEA Schedule CII
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LISDEXAMFETAMINE DIMESYLATE(UNII: SJT761GEGS)
(LISDEXAMFETAMINE - UNII:H645GUL8KJ) 		LISDEXAMFETAMINE DIMESYLATE30 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
MALTODEXTRIN(UNII: 7CVR7L4A2D)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
GUAR GUM(UNII: E89I1637KE)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MANNITOL(UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE)(UNII: 461P5CJN6T)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
SUCRALOSE(UNII: 96K6UQ3ZD4)
Product Characteristics
Color white (White to off white) Score no score
Shape TRIANGLE Size 11 mm
Flavor STRAWBERRY Imprint Code 30;S85
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:57664-085-88100 in 1 BOTTLE Type 0: Not a Combination Product25/08/2023
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA214134 08/25/2023
LISDEXAMFETAMINE DIMESYLATELISDEXAMFETAMINE DIMESYLATE TABLET, CHEWABLE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57664-086
Route of Administration ORAL DEA Schedule CII
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LISDEXAMFETAMINE DIMESYLATE(UNII: SJT761GEGS)
(LISDEXAMFETAMINE - UNII:H645GUL8KJ) 		LISDEXAMFETAMINE DIMESYLATE40 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
MALTODEXTRIN(UNII: 7CVR7L4A2D)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
GUAR GUM(UNII: E89I1637KE)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MANNITOL(UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE)(UNII: 461P5CJN6T)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
SUCRALOSE(UNII: 96K6UQ3ZD4)
Product Characteristics
Color white (White to off white) Score no score
Shape CAPSULE Size 14 mm
Flavor STRAWBERRY Imprint Code 40;S86
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:57664-086-88100 in 1 BOTTLE Type 0: Not a Combination Product25/08/2023
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA214134 08/25/2023
LISDEXAMFETAMINE DIMESYLATELISDEXAMFETAMINE DIMESYLATE TABLET, CHEWABLE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57664-087
Route of Administration ORAL DEA Schedule CII
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LISDEXAMFETAMINE DIMESYLATE(UNII: SJT761GEGS)
(LISDEXAMFETAMINE - UNII:H645GUL8KJ) 		LISDEXAMFETAMINE DIMESYLATE50 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
MALTODEXTRIN(UNII: 7CVR7L4A2D)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
GUAR GUM(UNII: E89I1637KE)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MANNITOL(UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE)(UNII: 461P5CJN6T)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
SUCRALOSE(UNII: 96K6UQ3ZD4)
Product Characteristics
Color white (White to off white) Score no score
Shape SQUARE (arc) Size 10 mm
Flavor STRAWBERRY Imprint Code 50;S87
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:57664-087-88100 in 1 BOTTLE Type 0: Not a Combination Product25/08/2023
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA214134 08/25/2023
LISDEXAMFETAMINE DIMESYLATELISDEXAMFETAMINE DIMESYLATE TABLET, CHEWABLE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57664-088
Route of Administration ORAL DEA Schedule CII
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LISDEXAMFETAMINE DIMESYLATE(UNII: SJT761GEGS)
(LISDEXAMFETAMINE - UNII:H645GUL8KJ) 		LISDEXAMFETAMINE DIMESYLATE60 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
MALTODEXTRIN(UNII: 7CVR7L4A2D)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
GUAR GUM(UNII: E89I1637KE)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MANNITOL(UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE)(UNII: 461P5CJN6T)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
SUCRALOSE(UNII: 96K6UQ3ZD4)
Product Characteristics
Color white (White to off white) Score no score
Shape DIAMOND Size 14 mm
Flavor STRAWBERRY Imprint Code 60;S88
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:57664-088-88100 in 1 BOTTLE Type 0: Not a Combination Product25/08/2023
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA214134 08/25/2023

LABELER - Sun Pharmaceutical Industries, Inc.(146974886)

Establishment
Name Address ID/FEI Business Operations
Ohm Laboratories Inc. 184769029 manufacture(57664-083, 57664-084, 57664-085, 57664-086, 57664-087, 57664-088, 57664-046, 57664-047, 57664-048, 57664-049, 57664-050, 57664-051, 57664-052)

PRINCIPAL DISPLAY PANEL

PDP Caps-10mg

PRINCIPAL DISPLAY PANEL

PDP Caps - 20mg

PRINCIPAL DISPLAY PANEL

PDP Caps-30mg

PRINCIPAL DISPLAY PANEL

PDP Caps - 40mg

PRINCIPAL DISPLAY PANEL

PDP Caps - 50mg

PRINCIPAL DISPLAY PANEL

PDP Caps - 60mg

PRINCIPAL DISPLAY PANEL

PDP Caps-70mg

PRINCIPAL DISPLAY PANEL

PDP-Chew-10mg

PRINCIPAL DISPLAY PANEL

PDP-Chew-20mg

PRINCIPAL DISPLAY PANEL

PDP-Chew-30mg

PRINCIPAL DISPLAY PANEL

PDP-Chew-40mg

PRINCIPAL DISPLAY PANEL

PDP-Chew-50mg

PRINCIPAL DISPLAY PANEL

PDP-Chew-60mg