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"57664-002-13" National Drug Code (NDC)

Pramipexole 500 TABLET in 1 BOTTLE (57664-002-13)
(Caraco Pharmaceutical Laboratories, Ltd.)

NDC Code57664-002-13
Package Description500 TABLET in 1 BOTTLE (57664-002-13)
Product NDC57664-002
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePramipexole
Non-Proprietary NamePramipexole
Dosage FormTABLET
UsageORAL
Start Marketing Date20130523
End Marketing Date20181228
Marketing Category NameANDA
Application NumberANDA091683
ManufacturerCaraco Pharmaceutical Laboratories, Ltd.
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/57664-002-13





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