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"16714-920-01" National Drug Code (NDC)
Pramipexole Dihydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-920-01)
(NorthStar RxLLC)
NDC Code
16714-920-01
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-920-01)
Product NDC
16714-920
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
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/16714-920-01