Veterinary Adverse Drug Reaction, Lack of Effectiveness, Product Defect Report, and Transmittal of Periodic Reports and Promotional Material for New Animal Drugs -- 21 CFR Part 510

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Information Collection (IC) Details

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IC Title:	Veterinary Adverse Drug Reaction, Lack of Effectiveness, Product Defect Report, and Transmittal of Periodic Reports and Promotional Material for New Animal Drugs -- 21 CFR Part 510	Agency IC Tracking Number:

Is this a Common Form? No		IC Status: Migrated

Obligation to Respond: Required to Obtain or Retain Benefits

CFR Citation:

Information Collection Instruments:

Document Type	Form No.	Available Electronically?	Can Be Submitted Electronically?
Form	FDA-1932	No	No
Form	FDA-1932A	No	No
Form	FDA-2301	No	No

Line of Business:

Subfunction:

Privacy Act System of Records
Title:	FR Citation:

Number of Respondents: 290	Number of Respondents for Small Entity: 0

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

Percentage of Respondents Reporting Electronically: 0 %

	Approved	Program Change Due to Agency Discretion
Annual Number of Responses for this IC	6,750	6,750
Annual IC Time Burden (Hours)	45,137	45,137
Annual IC Cost Burden (Dollars)	0	0

Documents for IC

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