Information Collection

Good Manufacturing Practice for Type A Medicated Articles, 21 CFR Part 226

IC 5766 under ICR 200107-0910-006 · OMB 0910-0154.

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0154 can be found here:

Documents and Forms

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Information Collection (IC) Details

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IC Title:	Good Manufacturing Practice for Type A Medicated Articles, 21 CFR Part 226	Agency IC Tracking Number:

Is this a Common Form? No		IC Status: Migrated

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

Line of Business:

Subfunction:

Privacy Act System of Records
Title:	FR Citation:

Number of Respondents: 115	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	Change Due to Adjustment in Agency Estimate	Previously Approved
Annual Number of Responses for this IC	180,550	36,550	144,000
Annual IC Time Burden (Hours)	187,450	37,450	150,000
Annual IC Cost Burden (Dollars)	0	0	0

Documents for IC

Title	Document	Date Uploaded

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