FR 9/30/97 Natural Rubber-Containing Medical Devices; User Labeling
...Device container vials with dry natural rubber stoppers, when used in combination with a drug.....At this time, the agency anticipates that the Drug/Device Intercenter Agreement will be amended.....The Packaging of This Product Contains Natural Rubber Latex Which May Cause Allergic..
http://www.fda.gov/cdrh/dsma/fr93097.html (score=100)

MDI and DPI Drug Products
...The guidance sets forth information that should be provided to ensure continuing drug.....elastomeric, plastic components or coatings of the container and closure system when in.....DPIs, the formulation, and the device with all of its parts including any protective..
http://www.fda.gov/cder/guidance/2180dft.pdf (score=46)

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