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INDUSTRY LETTER

Implementation Plan USP injection nomenclature March 1998

Final
Issued by:
Guidance Issuing Office
Center for Drug Evaluation and Research

The purpose of this letter from CDER is to provide you with the plan that CDER is using to implement the new injectable product nomenclature that became official in the United States Pharmacopeia.


Submit Comments

Submit comments on this guidance document electronically via docket ID: FDA-2013-S-0610 - Specific Electronic Submissions Intended For FDA's Dockets Management Staff (i.e., Citizen Petitions, Draft Proposed Guidance Documents, Variances, and other administrative record submissions)

If unable to submit comments online, please mail written comments to:

Dockets Management
Food and Drug Administration
5630 Fishers Lane, Rm 1061
Rockville, MD 20852

All comments should be identified with the title of the guidance.