NDC 59762-2420-07 - Doxazosin mesylate

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
59762-2420
Requested NDC
59762-2420-07
Package NDCs from labels
59762-2420-7, 59762-2420-07
Manufacturer
Mylan Pharmaceuticals Inc.
Effective date
2022-01-20
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Doxazosin mesylate - Mylan Pharmaceuticals Inc.Mylan Pharmaceuticals Inc.2022-01-20HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59762-2420-7Doxazosin100 in 1 BOTTLETABLET10018

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59762-2420DOXAZOSIN MESYLATE TABLET DOXAZOSIN TABLET [MYLAN PHARMACEUTICALS INC.]17Current NDC, Legacy NDC, 1 package rows20250511_6b887aa5-5edf-48c5-a480-dea8c35afa9d.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59762-2420-7EA - Each59762-2420eeb9b45d-259e-41ba-bb1a-eb31636b753f12021-11-09

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DOXAZOSIN MESYLATEACTIVE INGREDIENT86P6PQK0MUDOXAZOSIN MESYLATE TABLET [GREENSTONE LLC]2
DOXAZOSINACTIVE MOIETYNW1291F1W8DOXAZOSIN MESYLATE TABLET [GREENSTONE LLC]2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UDOXAZOSIN MESYLATE TABLET [GREENSTONE LLC]2
D&C YELLOW NO. 10INACTIVE INGREDIENT35SW5USQ3GDOXAZOSIN MESYLATE TABLET [GREENSTONE LLC]2
FD&C YELLOW NO. 6INACTIVE INGREDIENTH77VEI93A8DOXAZOSIN MESYLATE TABLET [GREENSTONE LLC]2
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GDOXAZOSIN MESYLATE TABLET [GREENSTONE LLC]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30DOXAZOSIN MESYLATE TABLET [GREENSTONE LLC]2
SODIUM LAURYL SULFATEINACTIVE INGREDIENT368GB5141JDOXAZOSIN MESYLATE TABLET [GREENSTONE LLC]2
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2DOXAZOSIN MESYLATE TABLET [GREENSTONE LLC]2

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 5 · 92 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DoxazosinDOXAZOSINREMEDYREPACK INC.30a6bb83-f91b-4c4f-a849-4f2be3735a0e2026-08-14Warnings, Adverse reactionsExact identifier
rxcui: 197626
unii: 86P6PQK0MU
DoxazosinDOXAZOSINMajor Pharmaceuticals3354196f-bbcf-4bc5-94f6-e6e8e132acb12026-08-05Warnings, Adverse reactionsExact identifier
rxcui: 197625
rxcui: 197626
rxcui: 197627
unii: 86P6PQK0MU
DoxazosinDOXAZOSINREMEDYREPACK INC.71815e8f-33ed-4f36-a8ec-d4443151a9d82026-07-08Warnings, Adverse reactionsExact identifier
rxcui: 197626
unii: 86P6PQK0MU
DoxazosinDOXAZOSINGolden State Medical Supply, Inc.54eeef3d-c906-37e7-e063-6294a90afca22026-06-23Warnings, Adverse reactionsExact identifier
rxcui: 197625
rxcui: 197628
rxcui: 197626
rxcui: 197627
unii: 86P6PQK0MU
DoxazosinDOXAZOSINREMEDYREPACK INC.bf2f7b41-f14d-4fcd-8db3-f507ca6ff78b2026-06-12Warnings, Adverse reactionsExact identifier
rxcui: 197627
unii: 86P6PQK0MU
DoxazosinDOXAZOSINREMEDYREPACK INC.ec06f008-37a1-4757-a3ee-0b4720912bc42026-06-11Warnings, Adverse reactionsExact identifier
rxcui: 197626
unii: 86P6PQK0MU
DoxazosinDOXAZOSINPD-Rx Pharmaceuticals, Inc.2ea9bb6b-a4f0-496a-b27b-4454167a4b702026-05-13Warnings, Adverse reactionsExact identifier
rxcui: 197626
unii: 86P6PQK0MU
DoxazosinDOXAZOSINCardinal Health 107, LLC08521333-ff21-45ad-b99e-1f43d945d24d2026-04-24Warnings, Adverse reactionsExact identifier
rxcui: 197626
unii: 86P6PQK0MU
DoxazosinDOXAZOSIN MESYLATEBryant Ranch Prepack277c3278-4fe2-47ac-9115-15b417325ffd2026-04-13Warnings, Adverse reactionsExact identifier
rxcui: 197627
unii: 86P6PQK0MU
DoxazosinDOXAZOSINPreferred Pharmaceuticals Inc.2110eec5-949d-4718-ad6d-3629e5db8a072026-04-08Warnings, Adverse reactionsExact identifier
rxcui: 197627
unii: 86P6PQK0MU
DoxazosinDOXAZOSINPreferred Pharmaceuticals Inc.e046e0b7-f510-4318-9884-034d683864d42026-04-08Warnings, Adverse reactionsExact identifier
rxcui: 197626
unii: 86P6PQK0MU
DoxazosinDOXAZOSINAvPAKde9ab9a4-d8b8-8b36-e053-2a95a90aaa352026-03-24Warnings, Adverse reactionsExact identifier
rxcui: 197625
rxcui: 197628
rxcui: 197626
rxcui: 197627
unii: 86P6PQK0MU
DoxazosinDOXAZOSINAvKAREe3d381c1-3b2f-af70-f4e6-08d6202eed252026-03-24Warnings, Adverse reactionsExact identifier
rxcui: 197628
rxcui: 197626
rxcui: 197627
unii: 86P6PQK0MU
DoxazosinDOXAZOSIN MESYLATEBryant Ranch Prepacke2f5d7d2-21aa-4921-8035-da945d3c565c2026-03-04Warnings, Adverse reactionsExact identifier
rxcui: 197627
unii: 86P6PQK0MU
DoxazosinDOXAZOSINNuCare Pharmaceuticals, Inc.54116886-ea5e-5320-e054-00144ff8d46c2026-02-16Warnings, Adverse reactionsExact identifier
rxcui: 197626
unii: 86P6PQK0MU
DoxazosinDOXAZOSIN MESYLATEBryant Ranch Prepack8641cdb1-dc16-4a13-8a84-bc8f6d58b4d42026-02-13Warnings, Adverse reactionsExact identifier
rxcui: 197626
unii: 86P6PQK0MU
DoxazosinDOXAZOSINBryant Ranch Prepack54549d19-6311-4dbb-8622-fd3e5440551a2026-01-29Warnings, Adverse reactionsExact identifier
rxcui: 197627
unii: 86P6PQK0MU
DoxazosinDOXAZOSINNorthwind Health Company, LLCf2b35586-d550-3fcb-e053-2995a90a34032026-01-19Warnings, Adverse reactionsExact identifier
rxcui: 197627
unii: 86P6PQK0MU
DoxazosinDOXAZOSIN MESYLATENorthwind Health Company, LLCf6c9856e-9154-f349-e053-6294a90a9f2c2026-01-19Warnings, Adverse reactionsExact identifier
rxcui: 197627
unii: 86P6PQK0MU
DoxazosinDOXAZOSINNorthwind Health Company, LLCf306adae-a2fe-5477-e053-2995a90a78382026-01-01Warnings, Adverse reactionsExact identifier
rxcui: 197625
unii: 86P6PQK0MU

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.