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"57664-004-18" National Drug Code (NDC)
Pramipexole 1000 TABLET in 1 BOTTLE (57664-004-18)
(Caraco Pharmaceutical Laboratories, Ltd.)
NDC Code
57664-004-18
Package Description
1000 TABLET in 1 BOTTLE (57664-004-18)
Product NDC
57664-004
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Pramipexole
Non-Proprietary Name
Pramipexole
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20130523
End Marketing Date
20181228
Marketing Category Name
ANDA
Application Number
ANDA091683
Manufacturer
Caraco Pharmaceutical Laboratories, Ltd.
Substance Name
PRAMIPEXOLE DIHYDROCHLORIDE
Strength
1
Strength Unit
mg/1
Pharmacy Classes
Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/57664-004-18