§207.37. What restrictions pertain to the use of the NDC? — Inbound Citations
21 C.F.R. § 207.37
Statutory Authority
Cited by 1 regulation in release Current.
Citations to 21 C.F.R. § 207.37 as a whole
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(b) FDA's acceptance of registration and listing information, inclusion of a drug in our database of drugs, or assignment of an NDC does not denote approval of the establishment or the drug or any other drugs of the establishment, nor does it mean that the drug may be legally marketed. Any representation that creates the impression that a drug is approved or is legally marketable because it appears in our database of drugs, has been assigned or displays an NDC, or the establishment has been assigned an establishment registration number or Unique Facility Identifier is misleading and constitutes misbranding. Failure to comply with § 207.37 may also constitute misbranding.