FDA.reportPublic FDA data

Phenazopyridine Hydrochloride

Product NDC
71205-999
Requested package NDC
71205-999-96
11-digit product format
712050999
Labeler code
71205
Product ID
71205-999_a4c41d5c-157d-4350-a4b3-b61f9650372d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Phenazopyridine Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Proficient Rx LP
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2016-11-10
Marketing end
0000-00-00
Substance
PHENAZOPYRIDINE HYDROCHLORIDE
Active strength
200 mg/1
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage71205-99971205-999-96DDiscontinued by firm2026-10-16

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage71205-99971205-999-96DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage71205-99971205-999-96DDiscontinued by firmexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71205-999-00EA - Each71205-999b440f1ad-c2fc-4e38-a872-4a4ab75c736c12021-06-02
71205-999-06EA - Each71205-999faa938c7-2f7a-4ff8-946e-def2e1cc637012021-06-02
71205-999-10EA - Each71205-999f2b3235c-09ec-43a3-a058-35609249227612021-06-02
71205-999-12EA - Each71205-999f5a9276c-367d-49b9-9d9b-b18f0ebc008812021-06-02
71205-999-20EA - Each71205-9990d912296-4333-48a6-bcd2-98e06dfa34aa12021-06-02
71205-999-24EA - Each71205-999b15dc71b-4ce8-43e0-b500-3b2425711adf12021-06-02
71205-999-55EA - Each71205-999f26b6299-30b2-4c34-a803-7d538c7fe58412021-06-02
71205-999-90EA - Each71205-999288cf745-05dc-41d8-aa9a-9b51485d236012021-06-02
71205-999-96EA - Each71205-9991478952e-d08b-4c92-a47d-1f207e8127c712021-06-02

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71205-999PHENAZOPYRIDINE HYDROCHLORIDE TABLET, FILM COATED [PROFICIENT RX LP]3Legacy NDC20220412_2819a501-5ff9-4179-af83-e1a7c91636a7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71205-999-967120509999696 TABLET, FILM COATED in 1 BOTTLE (71205-999-96) 2019-12-190000-00-00NoNoCurrent