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"57664-224-88" National Drug Code (NDC)
Oxycodone Hydrochloride 100 TABLET in 1 BOTTLE (57664-224-88)
(Sun Pharmaceutical Industries, Inc.)
NDC Code
57664-224-88
Package Description
100 TABLET in 1 BOTTLE (57664-224-88)
Product NDC
57664-224
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Oxycodone Hydrochloride
Non-Proprietary Name
Oxycodone Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20090512
Marketing Category Name
ANDA
Application Number
ANDA090659
Manufacturer
Sun Pharmaceutical Industries, Inc.
Substance Name
OXYCODONE HYDROCHLORIDE
Strength
30
Strength Unit
mg/1
Pharmacy Classes
Full Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA Schedule
CII
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/57664-224-88