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"52125-517-03" National Drug Code (NDC)
Dicyclomine Hydrochloride 20 TABLET in 1 VIAL (52125-517-03)
(REMEDYREPACK INC.)
NDC Code
52125-517-03
Package Description
20 TABLET in 1 VIAL (52125-517-03)
Product NDC
52125-517
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Dicyclomine Hydrochloride
Non-Proprietary Name
Dicyclomine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20130624
Marketing Category Name
ANDA
Application Number
ANDA085223
Manufacturer
REMEDYREPACK INC.
Substance Name
DICYCLOMINE HYDROCHLORIDE
Strength
20
Strength Unit
mg/1
Pharmacy Classes
Anticholinergic [EPC],Cholinergic Antagonists [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52125-517-03