Home NDC 23594-915 Veripred 20
Product NDC 23594-915
11-digit product format 235940915
Labeler code 23594
Product ID 23594-915_68731140-8dae-4952-9dea-79b4869c1f93
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name PREDNISOLONE SODIUM PHOSPHATE
Dosage form SOLUTION
Route ORAL
Labeler Cerecor, Inc.
Application ANDA078988
Marketing category ANDA
Marketing start 2014-08-01
Marketing end 0000-00-00
Substance PREDNISOLONE SODIUM PHOSPHATE
Active strength 20 mg/5mL
Pharmacologic classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag No
Listing certified through 2020-12-31
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 · 24 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 23594-915-08 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 23594-915-08 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 23594-915-08 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 23594-915-08 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 23594-915-08 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 23594-915-08 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 23594-915-08 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 23594-915-08 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 23594-915-08 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 23594-915-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 23594-915-08 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 23594-915-08 557ba5c1ecfa…9c80585c8c6e…
Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 1 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A078988-001 PREDNISOLONE SODIUM PHOSPHATE PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 1 matching rows.
Application-product, TE code table Application-product TE code A078988-001 AA
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Product history page 1 of 2 · 41 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-02-19 14:30 UTC 2026-02 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 1e350fbaab3a…2024-05-31 18:47 UTC 2024-05 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 8072bd15b7f6…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 5c6f7cd8ea54…2022-04-08 23:34 UTC 2022-04 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 5d02ea3f76ae…2022-04-04 05:41 UTC 2022-04 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 4b0b4de00fa7…2019-12-13 00:20 UTC 2019-12 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 74a2ff9319b5…2022-03-09 01:35 UTC 2022-03 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 bb7c543d1eb4…2021-12-28 21:50 UTC 2021-12 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 782e0a99824c…2021-05-05 16:15 UTC · 3 captures of this ZIP 2021-05 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 87673890dc5c…2021-03-12 10:30 UTC 2021-03 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 5aa47cf7b7d7…2020-12-22 03:56 UTC 2020-12 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 8869cabd3fbd…2020-11-12 02:37 UTC 2020-11 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 c0c555d07b60…2019-12-14 00:12 UTC 2019-12 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 3f01610625f2…2019-09-15 20:21 UTC 2019-09 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 b00525d2431f…2019-07-19 19:46 UTC 2019-07 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 ea99ee380514…2024-03-16 18:09 UTC · 4 captures of this ZIP 2024-03 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 6a51e52b5d6a…2024-02-18 07:12 UTC 2024-02 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 1c564ffb4f44…2023-12-20 04:57 UTC 2023-12 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 ea1830bbd6c7…2023-11-28 05:40 UTC · 2 captures of this ZIP 2023-11 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 a72a2bbeb626…2023-10-25 00:34 UTC · 2 captures of this ZIP 2023-10 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 9b2671bbb829…2023-07-15 15:27 UTC · 2 captures of this ZIP 2023-07 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 a67488948f0b…2023-06-13 01:57 UTC · 3 captures of this ZIP 2023-06 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 3f0d92c62455…2023-05-13 08:27 UTC 2023-05 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 053a50430f4f…2023-01-26 05:58 UTC 2023-01 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 3bdfa0b2c4d7…2022-11-12 20:34 UTC · 5 captures of this ZIP 2022-11 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 3a93d1ddd44b…2022-10-28 04:53 UTC 2022-10 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 f41ea6bd6efb…2022-09-29 23:25 UTC 2022-09 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 e64feba35796…2022-07-09 03:26 UTC · 3 captures of this ZIP 2022-07 A078988-001 PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML SOLUTION / ORAL AA RS 2008-06-09 cb3db0bc1861…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 2 · 41 observed states.
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded PREDNISOLONE SODIUM PHOSPHATE ACTIVE INGREDIENT IV021NXA9J VERIPRED 20 (PREDNISOLONE SODIUM PHOSPHATE) SOLUTION [ZYLERA PHARMACEUTICALS, LLC] 1 PREDNISOLONE ACTIVE MOIETY 9PHQ9Y1OLM VERIPRED 20 (PREDNISOLONE SODIUM PHOSPHATE) SOLUTION [ZYLERA PHARMACEUTICALS, LLC] 1 CORN SYRUP INACTIVE INGREDIENT 9G5L16BK6N VERIPRED 20 (PREDNISOLONE SODIUM PHOSPHATE) SOLUTION [ZYLERA PHARMACEUTICALS, LLC] 1 EDETATE DISODIUM INACTIVE INGREDIENT 7FLD91C86K VERIPRED 20 (PREDNISOLONE SODIUM PHOSPHATE) SOLUTION [ZYLERA PHARMACEUTICALS, LLC] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX VERIPRED 20 (PREDNISOLONE SODIUM PHOSPHATE) SOLUTION [ZYLERA PHARMACEUTICALS, LLC] 1 HYDROXYETHYL CELLULOSE (5000 CPS AT 1%) INACTIVE INGREDIENT X70SE62ZAR VERIPRED 20 (PREDNISOLONE SODIUM PHOSPHATE) SOLUTION [ZYLERA PHARMACEUTICALS, LLC] 1 METHYLPARABEN INACTIVE INGREDIENT A2I8C7HI9T VERIPRED 20 (PREDNISOLONE SODIUM PHOSPHATE) SOLUTION [ZYLERA PHARMACEUTICALS, LLC] 1 POTASSIUM PHOSPHATE, DIBASIC INACTIVE INGREDIENT CI71S98N1Z VERIPRED 20 (PREDNISOLONE SODIUM PHOSPHATE) SOLUTION [ZYLERA PHARMACEUTICALS, LLC] 1 POTASSIUM PHOSPHATE, MONOBASIC INACTIVE INGREDIENT 4J9FJ0HL51 VERIPRED 20 (PREDNISOLONE SODIUM PHOSPHATE) SOLUTION [ZYLERA PHARMACEUTICALS, LLC] 1 SACCHARIN SODIUM INACTIVE INGREDIENT SB8ZUX40TY VERIPRED 20 (PREDNISOLONE SODIUM PHOSPHATE) SOLUTION [ZYLERA PHARMACEUTICALS, LLC] 1 WATER INACTIVE INGREDIENT 059QF0KO0R VERIPRED 20 (PREDNISOLONE SODIUM PHOSPHATE) SOLUTION [ZYLERA PHARMACEUTICALS, LLC] 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.