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"0069-0070-01" National Drug Code (NDC)
Oxaliplatin 20 mL in 1 VIAL (0069-0070-01)
(Pfizer Laboratories Div Pfizer Inc.)
NDC Code
0069-0070-01
Package Description
20 mL in 1 VIAL (0069-0070-01)
Product NDC
0069-0070
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Oxaliplatin
Non-Proprietary Name
Oxaliplatin
Dosage Form
INJECTION, SOLUTION
Usage
INTRAVENOUS
Start Marketing Date
20120809
Marketing Category Name
ANDA
Application Number
ANDA091358
Manufacturer
Pfizer Laboratories Div Pfizer Inc.
Substance Name
OXALIPLATIN
Strength
5
Strength Unit
mg/mL
Pharmacy Classes
Platinum-based Drug [EPC],Platinum-containing Compounds [Chemical/Ingredient]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0069-0070-01