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"61919-371-14" National Drug Code (NDC)
Ciprofloxacin 14 TABLET in 1 BOTTLE (61919-371-14)
(Direct Rx)
NDC Code
61919-371-14
Package Description
14 TABLET in 1 BOTTLE (61919-371-14)
Product NDC
61919-371
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ciprofloxacin
Non-Proprietary Name
Ciprofloxacin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20140101
Marketing Category Name
ANDA
Application Number
ANDA076639
Manufacturer
Direct Rx
Substance Name
CIPROFLOXACIN HYDROCHLORIDE
Strength
250
Strength Unit
mg/1
Pharmacy Classes
Quinolone Antimicrobial [EPC],Quinolones [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-371-14