NDC SPL data elements

Sugammadex

INJECTION · HUMAN PRESCRIPTION DRUG · ANDA215701

83301-0078-2ANDA
Proprietary name
Sugammadex
Application number or citation
ANDA215701
Product type
HUMAN PRESCRIPTION DRUG
Marketing start date
20261102
Package NDC
83301-0078-2
Marketing category
ANDA
Package ndc11
83301007802
Dosage form
INJECTION
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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.