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"68084-308-21" National Drug Code (NDC)
Ropinirole Hydrochloride 3 BLISTER PACK in 1 CARTON (68084-308-21) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-308-11)
(American Health Packaging)
NDC Code
68084-308-21
Package Description
3 BLISTER PACK in 1 CARTON (68084-308-21) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-308-11)
Product NDC
68084-308
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
20130705
Marketing Category Name
ANDA
Application Number
ANDA079050
Manufacturer
American Health Packaging
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/68084-308-21