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Levothyroxine Sodium

Levothyroxine Sodium Tablets, USP

Approved
Approval ID

dc827fec-2b59-416f-b203-252c03b686d5

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Sep 9, 2009

Manufacturers
FDA

Rebel Distributors Corp.

DUNS: 118802834

Products 7

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Levothyroxine Sodium

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code21695-756
Application NumberNDA021210
Product Classification
M
Marketing Category
C73594
G
Generic Name
Levothyroxine Sodium
Product Specifications
Route of AdministrationORAL
Effective DateSeptember 9, 2009
FDA Product Classification

INGREDIENTS (10)

Levothyroxine SodiumActive
Quantity: 0.15 mg in 1 1
Code: 9J765S329G
Classification: ACTIM
Cellulose, MicrocrystallineInactive
Code: OP1R32D61U
Classification: IACT
Magnesium StearateInactive
Code: 70097M6I30
Classification: IACT
Silicon DioxideInactive
Code: ETJ7Z6XBU4
Classification: IACT
LactoseInactive
Code: J2B2A4N98G
Classification: IACT
Starch, CornInactive
Code: O8232NY3SJ
Classification: IACT
Aluminum OxideInactive
Code: LMI26O6933
Classification: IACT
Sodium Starch Glycolate Type A PotatoInactive
Code: 5856J3G2A2
Classification: IACT
AcaciaInactive
Code: 5C5403N26O
Classification: IACT
FD&C Blue No. 2Inactive
Code: L06K8R7DQK
Classification: IACT

Levothyroxine Sodium

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code21695-758
Application NumberNDA021210
Product Classification
M
Marketing Category
C73594
G
Generic Name
Levothyroxine Sodium
Product Specifications
Route of AdministrationORAL
Effective DateSeptember 9, 2009
FDA Product Classification

INGREDIENTS (10)

D&C Red No. 40Inactive
Code: WZB9127XOA
Classification: IACT
Silicon DioxideInactive
Code: ETJ7Z6XBU4
Classification: IACT
Cellulose, MicrocrystallineInactive
Code: OP1R32D61U
Classification: IACT
Magnesium StearateInactive
Code: 70097M6I30
Classification: IACT
Levothyroxine SodiumActive
Quantity: 0.2 mg in 1 1
Code: 9J765S329G
Classification: ACTIM
LactoseInactive
Code: J2B2A4N98G
Classification: IACT
Starch, CornInactive
Code: O8232NY3SJ
Classification: IACT
AcaciaInactive
Code: 5C5403N26O
Classification: IACT
Sodium Starch Glycolate Type A PotatoInactive
Code: 5856J3G2A2
Classification: IACT
Aluminum OxideInactive
Code: LMI26O6933
Classification: IACT

Levothyroxine Sodium

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code21695-750
Application NumberNDA021210
Product Classification
M
Marketing Category
C73594
G
Generic Name
Levothyroxine Sodium
Product Specifications
Route of AdministrationORAL
Effective DateSeptember 9, 2009
FDA Product Classification

INGREDIENTS (11)

Silicon DioxideInactive
Code: ETJ7Z6XBU4
Classification: IACT
Aluminum OxideInactive
Code: LMI26O6933
Classification: IACT
FD&C Blue No. 2Inactive
Code: L06K8R7DQK
Classification: IACT
Levothyroxine SodiumActive
Quantity: 0.075 mg in 1 1
Code: 9J765S329G
Classification: ACTIM
LactoseInactive
Code: J2B2A4N98G
Classification: IACT
Starch, CornInactive
Code: O8232NY3SJ
Classification: IACT
Sodium Starch Glycolate Type A PotatoInactive
Code: 5856J3G2A2
Classification: IACT
Cellulose, MicrocrystallineInactive
Code: OP1R32D61U
Classification: IACT
Magnesium StearateInactive
Code: 70097M6I30
Classification: IACT
AcaciaInactive
Code: 5C5403N26O
Classification: IACT
D&C Red No. 40Inactive
Code: WZB9127XOA
Classification: IACT

Levothyroxine Sodium

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code21695-754
Application NumberNDA021210
Product Classification
M
Marketing Category
C73594
G
Generic Name
Levothyroxine Sodium
Product Specifications
Route of AdministrationORAL
Effective DateSeptember 9, 2009
FDA Product Classification

INGREDIENTS (12)

LactoseInactive
Code: J2B2A4N98G
Classification: IACT
Magnesium StearateInactive
Code: 70097M6I30
Classification: IACT
Cellulose, MicrocrystallineInactive
Code: OP1R32D61U
Classification: IACT
D&C Red No. 40Inactive
Code: WZB9127XOA
Classification: IACT
Aluminum OxideInactive
Code: LMI26O6933
Classification: IACT
Levothyroxine SodiumActive
Quantity: 0.125 mg in 1 1
Code: 9J765S329G
Classification: ACTIM
Starch, CornInactive
Code: O8232NY3SJ
Classification: IACT
Silicon DioxideInactive
Code: ETJ7Z6XBU4
Classification: IACT
AcaciaInactive
Code: 5C5403N26O
Classification: IACT
Sodium Starch Glycolate Type A PotatoInactive
Code: 5856J3G2A2
Classification: IACT
D&C Blue No. 1Inactive
Code: H3R47K3TBD
Classification: IACT
D&C Yellow No. 6Inactive
Code: H77VEI93A8
Classification: IACT

Levothyroxine Sodium

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code21695-748
Application NumberNDA021210
Product Classification
M
Marketing Category
C73594
G
Generic Name
Levothyroxine Sodium
Product Specifications
Route of AdministrationORAL
Effective DateSeptember 9, 2009
FDA Product Classification

INGREDIENTS (10)

Levothyroxine SodiumActive
Quantity: 0.025 mg in 1 1
Code: 9J765S329G
Classification: ACTIM
Silicon DioxideInactive
Code: ETJ7Z6XBU4
Classification: IACT
LactoseInactive
Code: J2B2A4N98G
Classification: IACT
Magnesium StearateInactive
Code: 70097M6I30
Classification: IACT
Cellulose, MicrocrystallineInactive
Code: OP1R32D61U
Classification: IACT
Starch, CornInactive
Code: O8232NY3SJ
Classification: IACT
AcaciaInactive
Code: 5C5403N26O
Classification: IACT
Sodium Starch Glycolate Type A PotatoInactive
Code: 5856J3G2A2
Classification: IACT
D&C Yellow No. 6Inactive
Code: H77VEI93A8
Classification: IACT
Aluminum OxideInactive
Code: LMI26O6933
Classification: IACT

Levothyroxine Sodium

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code21695-752
Application NumberNDA021210
Product Classification
M
Marketing Category
C73594
G
Generic Name
Levothyroxine Sodium
Product Specifications
Route of AdministrationORAL
Effective DateSeptember 9, 2009
FDA Product Classification

INGREDIENTS (11)

Silicon DioxideInactive
Code: ETJ7Z6XBU4
Classification: IACT
Levothyroxine SodiumActive
Quantity: 0.1 mg in 1 1
Code: 9J765S329G
Classification: ACTIM
LactoseInactive
Code: J2B2A4N98G
Classification: IACT
Magnesium StearateInactive
Code: 70097M6I30
Classification: IACT
Cellulose, MicrocrystallineInactive
Code: OP1R32D61U
Classification: IACT
Starch, CornInactive
Code: O8232NY3SJ
Classification: IACT
AcaciaInactive
Code: 5C5403N26O
Classification: IACT
D&C Yellow No. 10Inactive
Code: 35SW5USQ3G
Classification: IACT
D&C Yellow No. 6Inactive
Code: H77VEI93A8
Classification: IACT
Sodium Starch Glycolate Type A PotatoInactive
Code: 5856J3G2A2
Classification: IACT
Aluminum OxideInactive
Code: LMI26O6933
Classification: IACT

Levothyroxine Sodium

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code21695-749
Application NumberNDA021210
Product Classification
M
Marketing Category
C73594
G
Generic Name
Levothyroxine Sodium
Product Specifications
Route of AdministrationORAL
Effective DateSeptember 9, 2009
FDA Product Classification

INGREDIENTS (8)

Levothyroxine SodiumActive
Quantity: 0.05 mg in 1 1
Code: 9J765S329G
Classification: ACTIM
Silicon DioxideInactive
Code: ETJ7Z6XBU4
Classification: IACT
LactoseInactive
Code: J2B2A4N98G
Classification: IACT
Magnesium StearateInactive
Code: 70097M6I30
Classification: IACT
AcaciaInactive
Code: 5C5403N26O
Classification: IACT
Cellulose, MicrocrystallineInactive
Code: OP1R32D61U
Classification: IACT
Starch, CornInactive
Code: O8232NY3SJ
Classification: IACT
Sodium Starch Glycolate Type A PotatoInactive
Code: 5856J3G2A2
Classification: IACT

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Levothyroxine Sodium - FDA Drug Approval Details