ANDA 216202

ZENARA

FDA Drug Application

Application #216202

Application Sponsors

ANDA 216202

ZENARA

Marketing Status

• Prescription: 001
• Prescription: 002

Application Products

001	TABLET;ORAL	EQ 5MG BASE	0	PROCHLORPERAZINE MALEATE	PROCHLORPERAZINE MALEATE
002	TABLET;ORAL	EQ 10MG BASE	0	PROCHLORPERAZINE MALEATE	PROCHLORPERAZINE MALEATE

FDA Submissions

UNKNOWN;

ORIG

1

AP

2022-06-13

STANDARD

Submissions Property Types

ORIG

1

Null

15

TE Codes

001	Prescription	AB
002	Prescription	AB

CDER Filings

Accessdata Error

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 216202
            [companyName] => Accessdata Error
            [docInserts] => ["",""]
            [products] => []
            [labels] => 
            [originalApprovals] => []
            [supplements] => 
            [actionDate] => 0000-00-00
        )

)