Selegiline Hydrochloride

Basic Information

Product Name

FDA Product Code

71205-888

Regulatory Information

NDC Product Code

71205-888

Application Number

ANDA206803

Marketing Category

C73584

Effective Date

April 1, 2022

Territorial Authority

USA

FDA Title

Selegiline Hydrochloride Capsules, 5mg

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Version Number

Active Ingredients

SELEGILINE HYDROCHLORIDE

Quantity: 5 mg in 1 1

Code: 6W731X367Q

Class Code: ACTIB

ANHYDROUS LACTOSE

Code: 3SY5LH9PMK

Class Code: IACT

ANHYDROUS CITRIC ACID

Code: XF417D3PSL

Class Code: IACT

SILICON DIOXIDE

Code: ETJ7Z6XBU4

Class Code: IACT

MICROCRYSTALLINE CELLULOSE

Code: OP1R32D61U

Class Code: IACT

MAGNESIUM STEARATE

Code: 70097M6I30

Class Code: IACT

Active Moieties

SELEGILINE

Code: 2K1V7GP655

Basic Information

Regulatory Information

Company Information

Active Ingredients

ANHYDROUS LACTOSE

ANHYDROUS CITRIC ACID

SILICON DIOXIDE

MICROCRYSTALLINE CELLULOSE

MAGNESIUM STEARATE

Active Moieties

SELEGILINE