Home NDC 49973-244-12 AZO
Product NDC 49973-244
Requested package NDC 49973-244-12
11-digit product format 499730244
Labeler code 49973
Product ID 49973-244_528926de-4ce1-4f6f-b805-1bbba3b45022
Type HUMAN OTC DRUG
Nonproprietary name Urinary Pain Relief
Dosage form TABLET
Route ORAL
Labeler i-Health, Inc.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2012-05-18
Marketing end 0000-00-00
Substance PHENAZOPYRIDINE HYDROCHLORIDE
Active strength 98 mg/1
NDC exclude flag No
Listing certified through 2021-12-31
Current FDA listing Historical FDA.report record 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 · 12 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…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Phenazopyridine Hydrochloride ACTIVE INGREDIENT 0EWG668W17 AZO (URINARY PAIN RELIEF) TABLET [I-HEALTH, INC.] 4 Phenazopyridine ACTIVE MOIETY K2J09EMJ52 AZO (URINARY PAIN RELIEF) TABLET [I-HEALTH, INC.] 4 CARNAUBA WAX INACTIVE INGREDIENT R12CBM0EIZ AZO (URINARY PAIN RELIEF) TABLET [I-HEALTH, INC.] 4 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U AZO (URINARY PAIN RELIEF) TABLET [I-HEALTH, INC.] 4 CROSCARMELLOSE SODIUM INACTIVE INGREDIENT M28OL1HH48 AZO (URINARY PAIN RELIEF) TABLET [I-HEALTH, INC.] 4 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO AZO (URINARY PAIN RELIEF) TABLET [I-HEALTH, INC.] 4 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 AZO (URINARY PAIN RELIEF) TABLET [I-HEALTH, INC.] 4 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A AZO (URINARY PAIN RELIEF) TABLET [I-HEALTH, INC.] 4 POVIDONE INACTIVE INGREDIENT FZ989GH94E AZO (URINARY PAIN RELIEF) TABLET [I-HEALTH, INC.] 4 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ AZO (URINARY PAIN RELIEF) TABLET [I-HEALTH, INC.] 4
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 49973-244-12 49973024412 6 BLISTER PACK in 1 BOX (49973-244-12) > 2 TABLET in 1 BLISTER PACK 6 blister pack 2012-05-18 0000-00-00 No No Current