Methylene Blue

Product NDC
17478-504
Requested package NDC
17478-504-10
11-digit product format
174780504
Labeler code
17478
Product ID
17478-504_59ee67a0-4203-459c-96f2-ef5af53a3bcc
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methylene Blue
Dosage form
INJECTION
Route
INTRAVENOUS
Labeler
Akorn
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2009-04-01
Marketing end
0000-00-00
Substance
METHYLENE BLUE
Active strength
10 mg/mL
Pharmacologic classes
Oxidation-Reduction Activity [MoA], Oxidation-Reduction Agent [EPC]
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 packagepackage17478-50417478-504-10DDiscontinued by firm2026-08-10

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 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…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
17478-504-01ML - Milliliter17478-5041abf5377-2a8c-456f-89d3-f77955d79be112012-07-24
17478-504-10ML - Milliliter17478-504dbc57c47-a817-470f-898d-b85eaab1772e12012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Methylene BlueACTIVE INGREDIENTT42P99266KMETHYLENE BLUE INJECTION, SOLUTION [GENERAL INJECTABLES & VACCINES, INC]1
Methylene BlueACTIVE INGREDIENTT42P99266KMETHYLENE BLUE INJECTION [AKORN, INC.]1
Methylene BlueACTIVE MOIETYT42P99266KMETHYLENE BLUE INJECTION, SOLUTION [GENERAL INJECTABLES & VACCINES, INC]1
Methylene BlueACTIVE MOIETYT42P99266KMETHYLENE BLUE INJECTION [AKORN, INC.]1
Hydrochloric AcidINACTIVE INGREDIENTQTT17582CBMETHYLENE BLUE INJECTION [AKORN, INC.]1
Sodium HydroxideINACTIVE INGREDIENT55X04QC32IMETHYLENE BLUE INJECTION [AKORN, INC.]1
WaterINACTIVE INGREDIENT059QF0KO0RMETHYLENE BLUE INJECTION [AKORN, INC.]1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
17478-504-101747805041010 VIAL in 1 CARTON (17478-504-10) > 10 mL in 1 VIAL10 vial2009-04-010000-00-00NoNoCurrent