"70771-1739-3" National Drug Code (NDC)

Pregabalin 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1739-3)
(Zydus Lifesciences Limited)

NDC Code70771-1739-3
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1739-3)
Product NDC70771-1739
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePregabalin
Non-Proprietary NamePregabalin
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20250412
Marketing Category NameANDA
Application NumberANDA215577
ManufacturerZydus Lifesciences Limited
Substance NamePREGABALIN
Strength82.5
Strength Unitmg/1
DEA ScheduleCV

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