JD Supra

FDA Extends Deadline for Removal of NDC and NHRIC Numbers from Device Labeling and Packaging

On August 30, 2016, the US Food and Drug Administration (FDA) published final guidance in which the agency announced it does not intend to enforce its prohibition against the inclusion of National ...
PharmTech

FDA Proposes Longer National Drug Code

The change would impact every package and hundreds of systems. All product labeling that carries the National Drug Code (NDC) will need to be updated if FDA finalizes its proposed rule to expand the ...
MD&M East

FDA Stops Issuing NHRIC and NDC Codes for Devices

FDA says that to conform to change made under the Unique Device Identification (UDI) final rule, it has stopped issuing National Health Related Items Code (NHRIC) and National Drug Code (NDC) labeler ...
Yahoo Finance

BioStem Technologies, Inc. (OTC: BSEM) Announces Issuance of FDA Drug Establishment Registration Number and FDA Labeler Code to Wholly Owned Subsidiary BioStem Pharmaceuticals ...

OAKLAND PARK, FL--(Marketwired - Jun 2, 2016) - BioStem Technologies, Inc. ("BioStem" or the "Company") (OTC PINK: BSEM) announced today that the FDA has accepted and issued BioStem Pharmaceuticals, ...
PharmTech

FDA Proposes Electronic Registration for All Manufacturers and Drugs

A recent analysis found that 9000 marketed drugs are not in FDA's National Drug Code Directory. The US Food and Drug Administration needs an effective system for registering and tracking ...
Health Affairs

Managing Off-Label Drug Use

The Food and Drug Administration (FDA) authorizes the marketing of drugs only for uses that the manufacturer has demonstrated to be safe and effective. However, the FDA does not regulate medical ...