Information Collection

Section 680, Forms FDA 356h & 2567

IC 193380 under ICR 201006-0910-001 · OMB 0910-0338.

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0338 can be found here:

Documents and Forms

Documents and forms in this information collection
Document Name	Document Type
Form FDA 356h Section 680, Forms FDA 356h & 2567	Form and Instruction
FDA 356h Application to Market a New Drug, Biologic, or an Antibi 0338 FDA-356h 2007.doc	Form and Instruction

IC Title:

Section 680, Forms FDA 356h & 2567

Agency IC Tracking Number:

Is this a Common Form? No

IC Status: New

Obligation to Respond: Mandatory

CFR Citation: 21 CFR 601.2(a) 21 CFR 610.60 21 CFR 610.61 21 CFR 601.62

Information Collection Instruments:

table that charts list of instruments
Document Type	Form No.	Form Name	Instrument File	URL	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability
Form and Instruction	FDA 356h	Application to Market a New Drug, Biologic, or an Antibiotic Drug for Human Use	0338 FDA-356h 2007.doc		Yes	No	Fillable Printable

Line of Business: Health

Subfunction: Consumer Health and Safety

Privacy Act System of Records

Title:

FR Citation:

Number of Respondents: 23

Number of Respondents for Small Entity: 0

Affected Public: Private Sector

Private Sector: Businesses or other for-profits

Percentage of Respondents Reporting Electronically: 20 %

table that charts list of burden
	Approved	Change Due to Adjustment in Agency Estimate
Annual Number of Responses for this IC	10	10
Annual IC Time Burden (Hours)	20	20
Annual IC Cost Burden (Dollars)	0	0

Documents for IC

table that charts IC Documents
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.