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"65862-605-78" National Drug Code (NDC)

Pramipexole Dihydrochloride 10 BLISTER PACK in 1 CARTON (65862-605-78) / 10 TABLET in 1 BLISTER PACK (65862-605-10)
(Aurobindo Pharma Limited)

NDC Code65862-605-78
Package Description10 BLISTER PACK in 1 CARTON (65862-605-78) / 10 TABLET in 1 BLISTER PACK (65862-605-10)
Product NDC65862-605
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePramipexole Dihydrochloride
Non-Proprietary NamePramipexole Dihydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20121026
Marketing Category NameANDA
Application NumberANDA202633
ManufacturerAurobindo Pharma Limited
Substance NamePRAMIPEXOLE DIHYDROCHLORIDE
Strength.25
Strength Unitmg/1
Pharmacy ClassesDopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]

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