"68462-332-90" National Drug Code (NDC)

Pramipexole Dihydrochloride 90 TABLET in 1 BOTTLE (68462-332-90)
(Glenmark Pharmaceuticals Inc., USA)

NDC Code68462-332-90
Package Description90 TABLET in 1 BOTTLE (68462-332-90)
Product NDC68462-332
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePramipexole Dihydrochloride
Non-Proprietary NamePramipexole Dihydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20101008
Marketing Category NameANDA
Application NumberANDA090781
ManufacturerGlenmark Pharmaceuticals Inc., USA
Substance NamePRAMIPEXOLE DIHYDROCHLORIDE
Strength.5
Strength Unitmg/1
Pharmacy ClassesDopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]

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