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"68382-342-01" National Drug Code (NDC)
Ropinirole Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (68382-342-01)
(Zydus Pharmaceuticals (USA) Inc.)
NDC Code
68382-342-01
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (68382-342-01)
Product NDC
68382-342
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ropinirole Hydrochloride
Non-Proprietary Name
Ropinirole Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20090923
Marketing Category Name
ANDA
Application Number
ANDA090411
Manufacturer
Zydus Pharmaceuticals (USA) Inc.
Substance Name
ROPINIROLE HYDROCHLORIDE
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/68382-342-01