Phenazopyridine Hydrochloride

Product NDC
51293-802
11-digit product format
512930802
Labeler code
51293
Product ID
51293-802_6ec64d33-6f0c-4b44-b23a-ec06e912dd8d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Phenazopyridine
Dosage form
TABLET
Route
ORAL
Labeler
ECI Pharmaceuticals, LLC
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
51293-802-012026-01-22C16284748780-19d75b9cf-e1ec-f424-e053-dadaa90a57ce89bb4bd7-6914-4ea8-a2bd-3e70d6f44535
51293-802-012020-01-31C16284748780-19d75b9cf-e1ec-f424-e053-dadaa90a57ce89bb4bd7-6914-4ea8-a2bd-3e70d6f44535

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51293-802-01EA - Each51293-802374a6be6-43ce-4ee8-bc3b-352473b9267e12014-11-05

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51293-802PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [ECI PHARMACEUTICALS, LLC]1Legacy NDC20141021_89bb4bd7-6914-4ea8-a2bd-3e70d6f44535.zip