"65862-605-99" National Drug Code (NDC)

Pramipexole Dihydrochloride 1000 TABLET in 1 BOTTLE (65862-605-99)
(Aurobindo Pharma Limited)

NDC Code65862-605-99
Package Description1000 TABLET in 1 BOTTLE (65862-605-99)
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/65862-605-99