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FDA ANDA · ANDA208038

METHYLNALTREXONE BROMIDE

Sponsor: US GENERICS, STERILES

APPLICATION
ANDA208038
TYPE
ANDA
ROUTE
SUBCUTANEOUS
DOSAGE FORM
SOLUTION
MARKETING STATUS
None (Tentative Approval)

Products

METHYLNALTREXONE BROMIDENone (Tentative Approval)
METHYLNALTREXONE BROMIDE 12MG/0.6ML · SOLUTION · SUBCUTANEOUS

Approval history

2021-08-12UNKNOWN · Original · standardLetterTA
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Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.

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