ARCOS Registrant Handbook
Revised as of August 1997
Contact Information
Summary of Reporting Changes
PART I: GENERAL INFORMATION
1.1 WHAT IS ARCOS?
1.2 ARCOS’ RELATIONSHIP TO DRUG INVENTORY AUDIT
1.3 ARCOS’ RELATIONSHIP TO UNITED NATIONS
1.4 REPORTING: WHO and WHAT
1.5 WHO MUST NOT REPORT?
1.6 MULTIPLE REGISTRATIONS
2.1 GENERAL REPORTING REQUIREMENTS
2.2 RETAINING COPIES
2.3 REPORTING MEDIA
2.4 REPORTING FREQUENCY
2.5 TRANSMITTAL INFORMATION
2.6 ARCOS REGISTRANTS AND REPORTERS
2.7 CENTRAL REPORTING
3.1 REPORTING MEDIA TYPES
3.2 CONFORMING TO SPECIFICATIONS
3.3 LABELING MEDIA
3.4 PACKING MEDIA FOR MAILING
3.5 QUESTIONS
3.6 MANUAL REPORTING
3.7 MAGNETIC TAPE REPORTING
3.8 MAGNETIC DISKETTE REPORTING
PART II: REPORT PREPARATION - INTRODUCTION TO PART II
4.1 RECORD TYPES
4.2 CONTROL RECORD
4.3 CONTROL RECORD FORMAT
4.4 ARCOS REPORT
4.5 ARCOS INPUT STREAM EXAMPLES
5.1 TRANSACTION RECORD
5.2 DEA FORM 333: DUPLICATING DATA
5.3 REPORTING REGISTRANT NUMBER
5.4 TRANSACTION CODE
5.5 INVENTORY TRANSACTION CODES
5.6 ACQUISITION TRANSACTION CODES
5.7 DISPOSITION TRANSACTION CODES
5.8 MISCELLANEOUS TRANSACTION CODES
5.9 ACTION INDICATOR (Formerly DELETE INDICATOR)
5.10 NATIONAL DRUG CODE (NDC)
5.11 QUANTITY
5.12 UNIT CODE
5.13 ASSOCIATE REGISTRANT NUMBER
5.14 DEA ORDER FORM NUMBER
5.15 TRANSACTION DATE
5.16 CORRECTION TRANSACTION
5.17 STRENGTH
5.18 TRANSACTION IDENTIFIER
5.19 DOCUMENT IDENTIFIER
6.1 GENERAL
6.2 NARCOTICS
6.3 PSYCHOTROPICS
6.4 MANUFACTURING ACTIVITIES FOR CODES N, W, L, Q, J
PART III: SYSTEM OUTPUT
PART IV: REFERENCE - APPENDICES
Appendix 1
Appendix 2
Appendix 3
Appendix 4
Appendix 5
Glossary
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