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"0007-4885-13" National Drug Code (NDC)
Requip 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0007-4885-13)
(GlaxoSmithKline LLC)
NDC Code
0007-4885-13
Package Description
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0007-4885-13)
Product NDC
0007-4885
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Requip
Proprietary Name Suffix
Xl
Non-Proprietary Name
Ropinirole Hydrochloride
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20080630
End Marketing Date
20190930
Marketing Category Name
NDA
Application Number
NDA022008
Manufacturer
GlaxoSmithKline 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/0007-4885-13