From:             Michael E. Coughlin, President and CEO, ScriptPro
Date:              July 26, 2002
Re:                 Food and Drug Administration (FDA), HHS, Public Meeting

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Barcode Label Requirements for Human Drug Products
July 26, 2002, from 9 a.m. to 5 p.m.
Natcher Auditorium, Building 45
National Institutes of Health, Bethesda, MD

 

RECOMMENDATIONS FOR THE DEVELOPMENT OF A REGULATION ON BARCODE LABELING FOR HUMAN DRUG PRODUCTS, INCLUDING BIOLOGIC PRODUCTS

APPENDIX F - DIFFERENT 11-DIGIT NDCs PRODUCE SAME 10-DIGIT NDC

11-DIGIT NDC (1ST PRODUCT)
11-DIGIT NDC (2ND PRODUCT)
10-DIGIT NDC (SAME FOR BOTH)

11845011855 FAT BLOCKER PLUS TABLET
11845118505 CITRIMAX 500 PLUS TABLET
1184511855

52959010220 METRONIDAZOLE 500MG TABLET
52959102200 BETAMETHASONE VA 0.1% CREAM
5295910220

52959011330 BACITRACIN ZINC OINTMENT
52959113300 TRIAMCINOLONE 0.5% CREAM
5295911330

52959014103 ACETAMINOPHEN/COD ELIXIR
52959141003 PROMETHAZINE/CODEINE SYRUP
5295914103

52959014410 SULFAMETHOXAZOLE/TMP DS TAB
52959144100 SANTYL OINTMENT
5295914410

52959014420 SULFAMETHOXAZOLE/TMP DS TAB
52959144200 BACITRACIN ZINC OINTMENT
5295914420

52959014500 ISONIAZID 300MG TABLET
52959145000 FLUOCINONIDE 0.05% OINTMENT
5295914500

58016010321 AMOXICILLIN 250MG CAPSULE
58016103201 AMPICILLIN 125MG/5ML SUSP
5801610321

58016031421 NAPROXEN 250MG TABLET
58016314201 RETIN-A 0.05% CREAM
5801631421

58016075230 LOPERAMIDE 2MG CAPSULE
58016752300 BENZTROPINE MES 2MG TABLET
5801675230