FDA ANDA · ANDA077854
PRAMIPEXOLE DIHYDROCHLORIDE
Sponsor: NATCO
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APPLICATION
ANDA077854
TYPE
ANDA
ORIGINAL APPROVAL
2010-10-08
LATEST ACTION
2026-10-16
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued
Products
PRAMIPEXOLE DIHYDROCHLORIDEDiscontinued
PRAMIPEXOLE DIHYDROCHLORIDE 0.5MG · TABLET · ORAL
PRAMIPEXOLE DIHYDROCHLORIDEDiscontinued
PRAMIPEXOLE DIHYDROCHLORIDE 0.125MG · TABLET · ORAL
PRAMIPEXOLE DIHYDROCHLORIDEDiscontinued
PRAMIPEXOLE DIHYDROCHLORIDE 1MG · TABLET · ORAL
PRAMIPEXOLE DIHYDROCHLORIDEDiscontinued
PRAMIPEXOLE DIHYDROCHLORIDE 0.25MG · TABLET · ORAL
PRAMIPEXOLE DIHYDROCHLORIDEDiscontinued
PRAMIPEXOLE DIHYDROCHLORIDE 1.5MG · TABLET · ORAL
Approval history
2026-10-16Labeling · Supplement 12 · standardAP
2024-03-19Labeling · Supplement 11 · standardAP
2024-03-19Labeling · Supplement 9 · standardAP
2024-03-19Labeling · Supplement 7 · standardAP
2024-03-19Labeling · Supplement 8 · standardAP
2024-03-19Labeling · Supplement 6 · standardAP
2024-03-19Labeling · Supplement 4 · standardAP
2013-08-08Labeling · Supplement 2 · standardAP
2010-10-08OriginalAP
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