Guidance for industry : labeling for human prescription drug and biological products, implementing the new content and format requirements.
| Other author | Center for Drug Evaluation and Research (U.S.) |
| Other author | Center for Biologics Evaluation and Research (U.S.) |
| Format | Electronic |
| Publication Info | Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : Center for Biologics Evaluation and Research, [2006] |
| Description | 1 online resource (27 p.) |
| Supplemental Content | https://purl.fdlp.gov/GPO/LPS118713 |
| Subjects |
| Portion of title | Labeling for human prescription drug and biological products, implementing the new content and format requirements |
| General note | "Draft guidance." |
| General note | "Labeling." |
| General note | "January 2006." |
| General note | GPO Cataloging Record Distribution Program (CRDP). |
| GPO item number | 0499-T (online) |
| Govt. docs number | HE 20.4702:P 92/4/DRAFT |