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"69452-361-20" National Drug Code (NDC)
Ropinirole 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-361-20)
(Bionpharma Inc.)
NDC Code
69452-361-20
Package Description
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-361-20)
Product NDC
69452-361
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ropinirole
Non-Proprietary Name
Ropinirole
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20220915
Marketing Category Name
ANDA
Application Number
ANDA079229
Manufacturer
Bionpharma Inc.
Substance Name
ROPINIROLE HYDROCHLORIDE
Strength
4
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/69452-361-20