SPL MEDGUIDE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 70771-1676-7

Lenalidomide Capsules, 2.5 mg

28 Capsules

Rx only

NDC 70771-1677-7

Lenalidomide Capsules, 5 mg

28 Capsules

Rx only

NDC 70771-1678-7

Lenalidomide Capsules, 10 mg

28 Capsules

Rx only

NDC 70771-1679-8

Lenalidomide Capsules, 15 mg

21 Capsules

Rx only

NDC 70771-1680-8

Lenalidomide Capsules, 20 mg

21 Capsules

Rx only

NDC 70771-1681-8

Lenalidomide Capsules, 25 mg

21 Capsules

Rx only

LENALIDOMIDE
lenalidomide capsule

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC:70771-1677
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
LENALIDOMIDE (UNII: F0P408N6V4) (LENALIDOMIDE - UNII:F0P408N6V4)	LENALIDOMIDE	5 mg

Ingredient Name	Strength
Inactive Ingredients
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
GELATIN (UNII: 2G86QN327L)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
SHELLAC (UNII: 46N107B71O)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	WHITE (white opaque cap with white opaque body)	Score	no score
Shape	CAPSULE (capsule)	Size	11mm
Flavor		Imprint Code	1031
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70771-1677-7	28 in 1 BOTTLE; Type 0: Not a Combination Product	09/12/2022
2	NDC:70771-1677-1	100 in 1 BOTTLE; Type 0: Not a Combination Product	09/12/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
ANDA	ANDA210154	09/12/2022

LENALIDOMIDE
lenalidomide capsule

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC:70771-1678
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
LENALIDOMIDE (UNII: F0P408N6V4) (LENALIDOMIDE - UNII:F0P408N6V4)	LENALIDOMIDE	10 mg

Ingredient Name	Strength
Inactive Ingredients
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
GELATIN (UNII: 2G86QN327L)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
SHELLAC (UNII: 46N107B71O)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	WHITE (White opaque cap) , BLUE (Turquoise blue opaque body)	Score	no score
Shape	CAPSULE (capsule)	Size	16mm
Flavor		Imprint Code	1032
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70771-1678-7	28 in 1 BOTTLE; Type 0: Not a Combination Product	09/12/2022
2	NDC:70771-1678-1	100 in 1 BOTTLE; Type 0: Not a Combination Product	09/12/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
ANDA	ANDA210154	09/12/2022

LENALIDOMIDE
lenalidomide capsule

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC:70771-1679
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
LENALIDOMIDE (UNII: F0P408N6V4) (LENALIDOMIDE - UNII:F0P408N6V4)	LENALIDOMIDE	15 mg

Ingredient Name	Strength
Inactive Ingredients
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
D&C RED NO. 28 (UNII: 767IP0Y5NH)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
GELATIN (UNII: 2G86QN327L)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
SHELLAC (UNII: 46N107B71O)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	WHITE (White opaque cap) , BLUE (Light Blue opaque body)	Score	no score
Shape	CAPSULE (capsule)	Size	18mm
Flavor		Imprint Code	1033
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70771-1679-1	100 in 1 BOTTLE; Type 0: Not a Combination Product	09/12/2022
2	NDC:70771-1679-8	21 in 1 BOTTLE; Type 0: Not a Combination Product	09/12/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
ANDA	ANDA210154	09/12/2022

LENALIDOMIDE
lenalidomide capsule

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC:70771-1681
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
LENALIDOMIDE (UNII: F0P408N6V4) (LENALIDOMIDE - UNII:F0P408N6V4)	LENALIDOMIDE	25 mg

Ingredient Name	Strength
Inactive Ingredients
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
D&C RED NO. 28 (UNII: 767IP0Y5NH)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
GELATIN (UNII: 2G86QN327L)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
SHELLAC (UNII: 46N107B71O)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	WHITE (White opaque cap) , BLUE (Light Blue opaque body)	Score	no score
Shape	CAPSULE (capsule)	Size	22mm
Flavor		Imprint Code	1035
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70771-1681-1	100 in 1 BOTTLE; Type 0: Not a Combination Product	09/12/2022
2	NDC:70771-1681-8	21 in 1 BOTTLE; Type 0: Not a Combination Product	09/12/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
ANDA	ANDA210154	09/12/2022

LENALIDOMIDE
lenalidomide capsule

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC:70771-1676
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
LENALIDOMIDE (UNII: F0P408N6V4) (LENALIDOMIDE - UNII:F0P408N6V4)	LENALIDOMIDE	2.5 mg

Ingredient Name	Strength
Inactive Ingredients
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
GELATIN (UNII: 2G86QN327L)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
SHELLAC (UNII: 46N107B71O)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	WHITE (white opaque cap with blue opaque body)	Score	no score
Shape	CAPSULE (capsule)	Size	11mm
Flavor		Imprint Code	1030
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70771-1676-7	28 in 1 BOTTLE; Type 0: Not a Combination Product	03/07/2023
2	NDC:70771-1676-1	100 in 1 BOTTLE; Type 0: Not a Combination Product	03/07/2023

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
ANDA	ANDA210154	03/07/2023

LENALIDOMIDE
lenalidomide capsule

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC:70771-1680
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
LENALIDOMIDE (UNII: F0P408N6V4) (LENALIDOMIDE - UNII:F0P408N6V4)	LENALIDOMIDE	20 mg

Ingredient Name	Strength
Inactive Ingredients
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
D&C RED NO. 28 (UNII: 767IP0Y5NH)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
GELATIN (UNII: 2G86QN327L)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
SHELLAC (UNII: 46N107B71O)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	BLUE (light blue opaque cap turquoise blue opaque body)	Score	no score
Shape	CAPSULE (capsule)	Size	19mm
Flavor		Imprint Code	1034
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70771-1680-8	21 in 1 BOTTLE; Type 0: Not a Combination Product	03/07/2023
2	NDC:70771-1680-1	100 in 1 BOTTLE; Type 0: Not a Combination Product	03/07/2023

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
ANDA	ANDA210154	03/07/2023

Labeler - Zydus Lifesciences Limited (918596198)

Name	Address	ID/FEI	Business Operations
Establishment
Zydus Lifesciences Limited		863362789	ANALYSIS(70771-1676, 70771-1677, 70771-1678, 70771-1679, 70771-1680, 70771-1681) , MANUFACTURE(70771-1676, 70771-1677, 70771-1678, 70771-1679, 70771-1680, 70771-1681)

LENALIDOMIDE capsules, for oral use

SPL MEDGUIDE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL