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"55648-771-02" National Drug Code (NDC)
Ropinirole Hydrochloride 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-771-02)
(Wockhardt Limited)
NDC Code
55648-771-02
Package Description
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-771-02)
Product NDC
55648-771
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ropinirole Hydrochloride
Non-Proprietary Name
Ropinirole Hydrochloride
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20120815
Marketing Category Name
ANDA
Application Number
ANDA091395
Manufacturer
Wockhardt Limited
Substance Name
ROPINIROLE HYDROCHLORIDE
Strength
2
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/55648-771-02