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"64679-771-04" National Drug Code (NDC)
Ropinirole Hydrochloride 10 BLISTER PACK in 1 CARTON (64679-771-04) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
(Wockhardt USA LLC.)
NDC Code
64679-771-04
Package Description
10 BLISTER PACK in 1 CARTON (64679-771-04) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC
64679-771
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 USA LLC.
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/64679-771-04