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"70518-2169-2" National Drug Code (NDC)
Phenazopyridine Hydrochloride 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2169-2)
(REMEDYREPACK INC.)
NDC Code
70518-2169-2
Package Description
21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2169-2)
Product NDC
70518-2169
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Phenazopyridine Hydrochloride
Non-Proprietary Name
Phenazopyridine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20190628
End Marketing Date
20240630
Marketing Category Name
UNAPPROVED DRUG OTHER
Manufacturer
REMEDYREPACK INC.
Substance Name
PHENAZOPYRIDINE HYDROCHLORIDE
Strength
200
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2169-2