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FDA ANDA · ANDA209182

NEOSTIGMINE METHYLSULFATE

Sponsor: AM REGENT

APPLICATION
ANDA209182
TYPE
ANDA
ORIGINAL APPROVAL
2018-05-04
LATEST ACTION
2021-11-12
ROUTE
INTRAVENOUS
DOSAGE FORM
SOLUTION
MARKETING STATUS
Discontinued

Products

NEOSTIGMINE METHYLSULFATEDiscontinued
NEOSTIGMINE METHYLSULFATE 10MG/10ML (1MG/ML) · SOLUTION · INTRAVENOUS
NEOSTIGMINE METHYLSULFATEDiscontinued
NEOSTIGMINE METHYLSULFATE 5MG/10ML (0.5MG/ML) · SOLUTION · INTRAVENOUS

Approval history

2021-11-12Labeling · Supplement 3 · standardAP
2018-05-04UNKNOWN · Original · standardAP
VIEW ON DRUGS@FDA ↗

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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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