← FDA Drug Approvals (Drugs@FDA)

OXYBUTYNIN CHLORIDE

ANDA · Abbreviated New Drug Application (Generic) · Sponsor: ABHAI LLC · Approved 2017-12-22

Drug application

FDA Application #

ANDA209335

Application type

Abbreviated New Drug Application (Generic)

Brand name

OXYBUTYNIN CHLORIDE

Generic name

OXYBUTYNIN CHLORIDE

Active ingredients

OXYBUTYNIN CHLORIDE

Dosage form

TABLET

Route

ORAL

Marketing status

Prescription

Sponsor

ABHAI LLC

Manufacturer

KVK-Tech, Inc.

First approval

2017-12-22

Source

Authoritative

Drugs@FDA application overview

Machine

JSON-LD · Markdown