Information Collection

Subpart B - Applications

IC 5662 under ICR 202003-0910-010 · OMB 0910-0001.

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0001 can be found here:

Documents and Forms

Documents and forms in this information collection
Document Name	Document Type
Form 356 Subpart B - Applications	Form
2252 instructions rev 2021.pdf	Instruction
FDA-2253-Instructions rev 2021.pdf	Instruction
PDUFA Committment Goals.pdf	Other-Performance Goals
FDARA 2017.pdf	Other-Legislative Authority
21 USC 355 New Drugs.pdf	Other-Statutory Authority
FDA 2252 Transmittal of annual drug and biologic report under 314 FDA 2252 reports rev 2021.pdf	Form
FDA 2253 TRANSMITTAL OF ADVERTISEMENTS AND PROMOTIONAL LABELING F FDA-2253 Transmittal rev 2021.pdf	Form
FDA 3542 Patent Information After Approval FDA 3542 patent info.pdf	Form and Instruction
FDA 3542a Patent Information Prior to Approval FDA-form-3542A_instructional-supplement_R2.1_secured.pdf	Form and Instruction
356 Application to Market a New or Abbreviated New Drug or B FORM 356h - 9-11-14.pdf	Form
FDA 3331a NDA - Field Alert Report Form FDA 3331a DRAFT FEB 2020.pdf www.fda.gov/drugs/surveillance/field-alert-reports	Form and Instruction

IC Title:

Subpart B - Applications

Agency IC Tracking Number:

Is this a Common Form? No

IC Status: Modified

Obligation to Respond: Mandatory

CFR Citation: 21 CFR 314.50-314.90

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	356	Application to Market a New or Abbreviated New Drug or Biologic for Human Use	FORM 356h - 9-11-14.pdf		Yes	Yes	Fillable Fileable
Form and Instruction	FDA 3331a	NDA - Field Alert Report	Form FDA 3331a DRAFT FEB 2020.pdf	https://www.fda.gov/drugs/surveillance/field-alert-reports	Yes	Yes	Fillable Fileable
Form	FDA 2252	Transmittal of annual drug and biologic report under 314.81	FDA 2252 reports rev 2021.pdf		Yes	Yes	Fillable Fileable
Instruction			2252 instructions rev 2021.pdf		Yes	Yes	Fillable Fileable
Form	FDA 2253	TRANSMITTAL OF ADVERTISEMENTS AND PROMOTIONAL LABELING FOR DRUGS AND BIOLOGICS FOR HUMAN USE	FDA-2253 Transmittal rev 2021.pdf		Yes	Yes	Fillable Fileable
Instruction			FDA-2253-Instructions rev 2021.pdf		Yes	Yes	Fillable Fileable
Other-Legislative Authority			FDARA 2017.pdf		Yes	Yes	Paper Only
Other-Performance Goals			PDUFA Committment Goals.pdf		Yes	Yes	Paper Only
Form and Instruction	FDA 3542	Patent Information After Approval	FDA 3542 patent info.pdf		Yes	Yes	Fillable Fileable
Form and Instruction	FDA 3542a	Patent Information Prior to Approval	FDA-form-3542A_instructional-supplement_R2.1_secured.pdf		Yes	Yes	Fillable Fileable
Other-Statutory Authority			21 USC 355 New Drugs.pdf		Yes	Yes	Fillable Fileable

Line of Business: Health

Subfunction: Public Health Monitoring

Privacy Act System of Records

Title:

FR Citation:

Number of Respondents: 378

Number of Respondents for Small Entity: 0

Affected Public: Private Sector

Private Sector: Businesses or other for-profits

Percentage of Respondents Reporting Electronically: 99 %

table that charts list of burden
	Requested	Change Due to Adjustment in Agency Estimate	Previously Approved
Annual Number of Responses for this IC	66,924	-4,782	71,706
Annual IC Time Burden (Hours)	1,234,195	-1,410,009	2,644,204
Annual IC Cost Burden (Dollars)	0	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.