NDC SPL data elements

Testosterone

GEL · HUMAN PRESCRIPTION DRUG · ANDA208620

21922-030-52ANDA
Proprietary name
Testosterone
Application number or citation
ANDA208620
Product type
HUMAN PRESCRIPTION DRUG
Marketing start date
20260601
Package NDC
21922-030-52
Marketing category
ANDA
Package ndc11
21922003052
Dosage form
GEL
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.