Phenazopyridine Hydrochloride

Product NDC: 63629-9127
Requested package NDC: 63629-9127-4
11-digit product format: 636299127
Labeler code: 63629
Product ID: 63629-9127_6e1d1e1d-6674-4916-9820-810ff883212c
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: 100 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
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	63629-9127	63629-9127-4	D	Discontinued by firm		2026-09-14

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 date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`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 NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63629-9127-1	EA - Each	63629-9127	7882cdc7-80ee-4529-8b03-0ef2a163d696	1	2022-01-06
63629-9127-2	EA - Each	63629-9127	32c14d1e-8c69-45a5-84d8-d30eae8e4980	1	2022-01-06
63629-9127-3	EA - Each	63629-9127	be06949f-7409-47ab-8cc6-aeacd8817237	1	2022-01-06
63629-9127-4	EA - Each	63629-9127	6c2b8697-37dd-459e-ab21-f2ea6e05ef6c	1	2022-01-06
63629-9127-5	EA - Each	63629-9127	721af957-2e2e-4148-ab83-9811dd0a9129	1	2022-01-06

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
0EWG668W17	PHENAZOPYRIDINE HYDROCHLORIDE	136-40-3	PHENAZOPYRIDINE HYDROCHLORIDE
K2J09EMJ52	PHENAZOPYRIDINE	94-78-0	Phenazopyridine

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63629-9127-4	63629912704	9 TABLET in 1 BOTTLE (63629-9127-4)	9 tablet	2021-12-06	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
PHENAZOPYRIDINE HYDROCHLORIDE TABLETS, USP Rx Only	Bryant Ranch Prepack	2023-10-25	HUMAN PRESCRIPTION DRUG LABEL	102

Phenazopyridine Hydrochloride

NDC auxiliary status#

Observed NDC auxiliary status history#

Reported adverse events (FAERS/openFDA)#

DailyMed Billing Units#

Related Records#

Related UNII Ingredients#

Packages#

Related DailyMed Labels#