Information Collection

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

IC 5767 under ICR 200712-0910-008 · OMB 0910-0154.

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Information Collection (IC) Details

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

Is this a Common Form? No		IC Status: Modified

Obligation to Respond: Mandatory

CFR Citation: 21 CFR 226.42 21 CFR 226.58 21 CFR 226.80 21 CFR 226.102 21 CFR 226.110 21 CFR 226.115

Information Collection Instruments:

Document Type	Form No.	Form Name	Instrument File	URL	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability

Line of Business: Health

Subfunction: Consumer Health and Safety

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	1,082,150	901,600	180,550
Annual IC Time Burden (Hours)	157,550	0	157,550
Annual IC Cost Burden (Dollars)	0	0	0

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