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"16714-921-01" National Drug Code (NDC)
Pramipexole Dihydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-921-01)
(NorthStar RxLLC)
NDC Code
16714-921-01
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-921-01)
Product NDC
16714-921
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Pramipexole Dihydrochloride
Non-Proprietary Name
Pramipexole Dihydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20190306
Marketing Category Name
ANDA
Application Number
ANDA206156
Manufacturer
NorthStar RxLLC
Substance Name
PRAMIPEXOLE DIHYDROCHLORIDE
Strength
3.75
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/16714-921-01