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"16571-413-05" National Drug Code (NDC)
Ciprofloxacin 50 TABLET in 1 BOTTLE (16571-413-05)
(Rising Pharma Holdings, Inc.)
NDC Code
16571-413-05
Package Description
50 TABLET in 1 BOTTLE (16571-413-05)
Product NDC
16571-413
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ciprofloxacin
Non-Proprietary Name
Ciprofloxacin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20040910
Marketing Category Name
ANDA
Application Number
ANDA076639
Manufacturer
Rising Pharma Holdings, Inc.
Substance Name
CIPROFLOXACIN HYDROCHLORIDE
Strength
750
Strength Unit
mg/1
Pharmacy Classes
Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/16571-413-05