NDC SPL data elements

Testosterone

SOLUTION · HUMAN PRESCRIPTION DRUG · ANDA212301

21922-109-16ANDA
Proprietary name
Testosterone
Application number or citation
ANDA212301
Product type
HUMAN PRESCRIPTION DRUG
Marketing start date
20260619
Package NDC
21922-109-16
Marketing category
ANDA
Package ndc11
21922010916
Dosage form
SOLUTION
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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.