Form FDA 356V

Reporting Associated with New Animal Drug Applications

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0032 can be found here:

Documents and Forms

Document Name Document Type
Form FDA 356V Form FDA 356V Form and Instruction
FDA 356V Application for Approval of a New Animal Drug (Or Submis 0032 FDA356V 5-1-13 ICR.pdf Form and Instruction

Information Collection (IC) Details

IC Title:	Form FDA 356V	Agency IC Tracking Number:

Is this a Common Form? No		IC Status: Removed

Obligation to Respond: Mandatory

CFR Citation:

Information Collection Instruments:

Document Type	Form No.	Form Name	Instrument File	URL	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability
Form and Instruction	FDA 356V	Application for Approval of a New Animal Drug (Or Submission to Support New Animal Drug Approval)	0032 FDA356V 5-1-13 ICR.pdf		Yes	Yes	Fillable Fileable

Line of Business: Health

Subfunction: Consumer Health and Safety

Privacy Act System of Records
Title:	FR Citation:

Number of Respondents: 169	Number of Respondents for Small Entity: 0

Affected Public: Private Sector	Private Sector: Businesses or other for-profits

Percentage of Respondents Reporting Electronically: 0 %

	Change Due to Adjustment in Agency Estimate	Previously Approved
Annual Number of Responses for this IC	-739	739
Annual IC Time Burden (Hours)	-3,695	3,695
Annual IC Cost Burden (Dollars)	0	0

Documents for IC

Title	Document	Date Uploaded
No associated records found

Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.