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"0069-1010-01" National Drug Code (NDC)
Oxaliplatin 20 mL in 1 VIAL (0069-1010-01)
(Pfizer Laboratories Div Pfizer Inc.)
NDC Code
0069-1010-01
Package Description
20 mL in 1 VIAL (0069-1010-01)
Product NDC
0069-1010
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Oxaliplatin
Non-Proprietary Name
Oxaliplatin
Dosage Form
POWDER, FOR SOLUTION
Usage
INTRAVENOUS
Start Marketing Date
20120809
Marketing Category Name
ANDA
Application Number
ANDA200979
Manufacturer
Pfizer Laboratories Div Pfizer Inc.
Substance Name
OXALIPLATIN
Strength
100
Strength Unit
mg/20mL
Pharmacy Classes
Platinum-based Drug [EPC],Platinum-containing Compounds [Chemical/Ingredient]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0069-1010-01