Phenazopyridine Hydrochloride

Product NDC
66116-484
11-digit product format
661160484
Labeler code
66116
Product ID
66116-484_a63d3ace-768f-4e1b-a5e9-dad1817453b9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Phenazopyridine
Dosage form
TABLET
Route
ORAL
Labeler
MedVantx, Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2011-02-01
Marketing end
0000-00-00
Substance
PHENAZOPYRIDINE HYDROCHLORIDE
Active strength
200 mg/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
66116-484-062019-11-13C16284748780-197449f38-cc20-f6ea-e053-dbdaa90aa703PHENAZOPYRIDINE HYDROCHLORIDE TABLETS, USP Rx Only

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66116-484-06Phenazopyridine Hydrochloride6 in 1 BOTTLETABLET61

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66116-484PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [MEDVANTX, INC.]1Legacy NDC, 1 package rows20120424_a63d3ace-768f-4e1b-a5e9-dad1817453b9.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1094104phenazopyridine HCl 200 MG Oral TabletPSNa63d3ace-768f-4e1b-a5e9-dad1817453b91
1094104phenazopyridine hydrochloride 200 MG Oral TabletSCDa63d3ace-768f-4e1b-a5e9-dad1817453b91

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
66116-484-06661160484066 in 1 BOTTLEHistorical