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"70518-3482-0" National Drug Code (NDC)
Ropinirole 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3482-0)
(REMEDYREPACK INC.)
NDC Code
70518-3482-0
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3482-0)
Product NDC
70518-3482
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ropinirole
Non-Proprietary Name
Ropinirole
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20220817
Marketing Category Name
ANDA
Application Number
ANDA090135
Manufacturer
REMEDYREPACK INC.
Substance Name
ROPINIROLE HYDROCHLORIDE
Strength
1
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/70518-3482-0