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Submission of Controlled Correspondence
Generic Drug User Fee Program
OMB: 0910-0727
IC ID: 262988
OMB.report
HHS/FDA
OMB 0910-0727
ICR 202411-0910-010
IC 262988
( )
Documents and Forms
Document Name
Document Type
0727 Competitive Generic Therapies Final guidance OCT 2022.pdf
Other-Agency Guidance
0727 Cover Letter Attachments for Controlled Correspondence and ANDA Submissions JUNE 2023.pdf
Other-Agency Guidance
0727 - CPAs draft guidance SEPT 2022.pdf
Other-Agency Guidance
0727 Formal Meetings Between FDA and ANDA Applicants of Complex Products Under GDUFA - OCT 2022.pdf
Other-Agency Guidance
0727 Controlled Correspondence draft DEC 2022.pdf
Other-Agency Guidance
0727 Product-Specific Guidance Meetings Between FDA and ANDA Applicants Under GDUFA.pdf
Other-Agency Guidance
Information Collection (IC) Details
View Information Collection (IC)
IC Title:
Submission of Controlled Correspondence
Agency IC Tracking Number:
Is this a Common Form?
No
IC Status:
Unchanged
Obligation to Respond:
Required to Obtain or Retain Benefits
CFR Citation:
21 CFR 10.115; Good guidance practice
21 CFR 314.445; Guidance documents
Information Collection Instruments:
Document Type
Form No.
Form Name
Instrument File
URL
Available Electronically?
Can Be Submitted Electronically?
Electronic Capability
Other-Agency Guidance
0727 Competitive Generic Therapies Final guidance OCT 2022.pdf
Yes
Yes
Fillable Fileable
Other-Agency Guidance
0727 Cover Letter Attachments for Controlled Correspondence and ANDA Submissions JUNE 2023.pdf
Yes
Yes
Fillable Fileable
Other-Agency Guidance
0727 - CPAs draft guidance SEPT 2022.pdf
Yes
Yes
Fillable Fileable
Other-Agency Guidance
0727 Formal Meetings Between FDA and ANDA Applicants of Complex Products Under GDUFA - OCT 2022.pdf
Yes
Yes
Fillable Fileable
Other-Agency Guidance
0727 Controlled Correspondence draft DEC 2022.pdf
Yes
Yes
Fillable Fileable
Other-Agency Guidance
0727 Product-Specific Guidance Meetings Between FDA and ANDA Applicants Under GDUFA.pdf
Yes
Yes
Fillable Fileable
Federal Enterprise Architecture Business Reference Module
Line of Business:
Health
Subfunction:
Consumer Health and Safety
Privacy Act System of Records
Title:
FR Citation:
Number of Respondents:
500
Number of Respondents for Small Entity:
0
Affected Public:
Private Sector
Private Sector:
Businesses or other for-profits
Percentage of Respondents Reporting Electronically:
0 %
Requested
Program Change Due to New Statute
Program Change Due to Agency Discretion
Change Due to Adjustment in Agency Estimate
Change Due to Potential Violation of the PRA
Previously Approved
Annual Number of Responses for this IC
5,000
0
0
0
0
5,000
Annual IC Time Burden (Hours)
25,000
0
0
0
0
25,000
Annual IC Cost Burden (Dollars)
0
0
0
0
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.