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"68788-8692-8" National Drug Code (NDC)
Ciprofloxacin 10 TABLET in 1 BOTTLE (68788-8692-8)
(Preferred Pharmaceuticals Inc.)
NDC Code
68788-8692-8
Package Description
10 TABLET in 1 BOTTLE (68788-8692-8)
Product NDC
68788-8692
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ciprofloxacin
Non-Proprietary Name
Ciprofolxacin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20240610
Marketing Category Name
ANDA
Application Number
ANDA208921
Manufacturer
Preferred Pharmaceuticals Inc.
Substance Name
CIPROFLOXACIN HYDROCHLORIDE
Strength
500
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/68788-8692-8