FdaApplication

NDA 016636

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Identifiers

Properties

PropertyValue
applicant_nameADAPT PHARMA OPERATIONS LTD
application_typeNDA
approval_date1982-06-14

Products (3)

ProductActive ingredientStrengthDosage form
NARCANNALOXONE HYDROCHLORIDE1MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**INJECTABLE;INJECTION
NARCANNALOXONE HYDROCHLORIDE0.4MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**INJECTABLE;INJECTION
NARCANNALOXONE HYDROCHLORIDE0.02MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**INJECTABLE;INJECTION

3 products