MedPath
FDA Product

Venlafaxine Hydrochloride

Product approved by U.S. Food and Drug Administration (US)

Basic Information

Venlafaxine Hydrochloride

53002-2361

Regulatory Information

53002-2361

ANDA200834

C73584

January 13, 2022

USA

These highlights do not include all the information needed to use VENLAFAXINE HYDROCHLORIDE EXTENDED-RELEASE CAPSULES safely and effectively. See full prescribing information for VENLAFAXINE HYDROCHLORIDE EXTENDED-RELEASE CAPSULES. VENLAFAXINE HYDROCHLORIDE extended-release capsules, for oral use Initial U.S. Approval: 1997

Human Prescription Drug Label

1

Company Information

147096275

Active Ingredients

HYPROMELLOSE 2910 (5 MPA.S)

Code: R75537T0T4

Class Code: IACT

ETHYLCELLULOSE (20 MPA.S)

Code: BJG0S321QY

Class Code: IACT

STARCH, CORN

Code: O8232NY3SJ

Class Code: IACT

VENLAFAXINE HYDROCHLORIDE

Quantity: 150 mg in 1 1

Code: 7D7RX5A8MO

Class Code: ACTIM

FERRIC OXIDE RED

Code: 1K09F3G675

Class Code: IACT

GELATIN, UNSPECIFIED

Code: 2G86QN327L

Class Code: IACT

SUCROSE

Code: C151H8M554

Class Code: IACT

FERROSOFERRIC OXIDE

Code: XM0M87F357

Class Code: IACT

SHELLAC

Code: 46N107B71O

Class Code: IACT

SODIUM LAURYL SULFATE

Code: 368GB5141J

Class Code: IACT

TALC

Code: 7SEV7J4R1U

Class Code: IACT

TITANIUM DIOXIDE

Code: 15FIX9V2JP

Class Code: IACT

Active Moieties

VENLAFAXINE

Code: GRZ5RCB1QG

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