Amoxapine

Basic Information

Product Name

Amoxapine

FDA Product Code

62135-701

Regulatory Information

NDC Product Code

62135-701

Application Number

ANDA072944

Marketing Category

C73584

Effective Date

September 8, 2023

Territorial Authority

USA

FDA Title

Amoxapine Tablets, USP Rx only

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Version Number

Active Ingredients

DIBASIC CALCIUM PHOSPHATE DIHYDRATE

Code: O7TSZ97GEP

Class Code: IACT

MICROCRYSTALLINE CELLULOSE

Code: OP1R32D61U

Class Code: IACT

STARCH, CORN

Code: O8232NY3SJ

Class Code: IACT

HYPROMELLOSE, UNSPECIFIED

Code: 3NXW29V3WO

Class Code: IACT

CROSCARMELLOSE SODIUM

Code: M28OL1HH48

Class Code: IACT

SODIUM STEARYL FUMARATE

Code: 7CV7WJK4UI

Class Code: IACT

AMOXAPINE

Quantity: 50 mg in 1 1

Code: R63VQ857OT

Class Code: ACTIB

Active Moieties

Code: R63VQ857OT

Amoxapine

Basic Information

Regulatory Information

Company Information

Active Ingredients

DIBASIC CALCIUM PHOSPHATE DIHYDRATE

MICROCRYSTALLINE CELLULOSE

STARCH, CORN

HYPROMELLOSE, UNSPECIFIED

CROSCARMELLOSE SODIUM

SODIUM STEARYL FUMARATE

Active Moieties

AMOXAPINE