FDA.reportPublic FDA data

Phenazopyridine Hydrochloride

Product NDC
71335-1805
Requested package NDC
71335-1805-3
11-digit product format
713351805
Labeler code
71335
Product ID
71335-1805_631af0ac-a2eb-4c6f-9e42-f6d39c6ca7c6
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Phenazopyridine
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2011-08-23
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 packagepackage71335-180571335-1805-3DDiscontinued by firm2026-10-15

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 · 11 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…

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
71335-1805-1EA - Each71335-1805fac3209a-fc0b-47b3-8018-384cc06e5b1212022-02-07
71335-1805-2EA - Each71335-180533d88523-799b-4156-9720-14ee9b075a1e12022-02-07
71335-1805-3EA - Each71335-1805e0e24c29-4193-4f25-9a4a-9b46199c1c6112021-11-09
71335-1805-4EA - Each71335-1805f3f5732d-667f-4d2f-a3c5-b9ea998c5c9712022-02-07
71335-1805-5EA - Each71335-1805645a58af-ea4d-41e7-aa5b-0290ec32811212021-06-02
71335-1805-6EA - Each71335-1805c128af29-655f-46d5-9bb8-fdf80994faf712021-06-02
71335-1805-7EA - Each71335-180539e8af38-24ac-46fc-8b15-09a309e94a5412021-11-09
71335-1805-8EA - Each71335-18050ef7c75f-8b3c-43e3-8a6d-ac6eabc68b2612022-01-06
71335-1805-9EA - Each71335-1805e86b0652-92ab-4b70-a086-772b5d2e6e0c12022-02-07

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1805-37133518050330 TABLET in 1 BOTTLE (71335-1805-3) 30 tablet2021-11-090000-00-00NoNoCurrent