FDA.reportPublic FDA data

NDC 68084-836-95 - Doxazosin

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
68084-836
Requested NDC
68084-836-95
Package NDCs from labels
68084-836-95, 68084-836-25, 68084-836-11, 68084-836-01
Manufacturer
American Health Packaging
Effective date
2025-09-17
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Doxazosin - American Health PackagingAmerican Health Packaging2025-09-17HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68084-836-01Doxazosin100 in 1 BOX, UNIT-DOSETABLET1009
68084-836-11Doxazosin1 in 1 BLISTER PACKTABLET19
68084-836-25Doxazosin30 in 1 BOX, UNIT-DOSETABLET309
68084-836-95Doxazosin1 in 1 BLISTER PACKTABLET19

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68084-836DOXAZOSIN TABLET [AMERICAN HEALTH PACKAGING]8Current NDC, Legacy NDC, 4 package rows20240229_3f4dc1a7-05e6-41d7-908c-30ce2677d87b.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68084-836-01EA - Each68084-836116333ec-e0b2-4a36-a56b-83fdefb742fc12020-07-13
68084-836-11EA - Each68084-836916b5902-ee5f-4008-bcf6-3b4c9ed75b4112014-11-05
68084-836-21EA - Each68084-8362176a02e-e1a3-4f28-a980-aa0d6b80cd2412014-11-05
68084-836-25EA - Each68084-8362988fb99-e02c-438e-86bf-77f68c91832612016-03-04
68084-836-95EA - Each68084-836f22c7ab1-34df-4e53-b754-90b230ee544712016-03-04

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DOXAZOSIN MESYLATEACTIVE INGREDIENT86P6PQK0MUDOXAZOSIN TABLET [AMERICAN HEALTH PACKAGING]1
DOXAZOSINACTIVE MOIETYNW1291F1W8DOXAZOSIN TABLET [AMERICAN HEALTH PACKAGING]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UDOXAZOSIN TABLET [AMERICAN HEALTH PACKAGING]1
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48DOXAZOSIN TABLET [AMERICAN HEALTH PACKAGING]1
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XDOXAZOSIN TABLET [AMERICAN HEALTH PACKAGING]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30DOXAZOSIN TABLET [AMERICAN HEALTH PACKAGING]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 4 of 4 · 67 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DoxazosinDOXAZOSINAphena Pharma Solutions - Tennessee, LLCb364c7a8-72b5-4776-a500-400c37a72c9b2022-02-03Warnings, Adverse reactionsExact identifier
unii: 86P6PQK0MU
DoxazosinDOXAZOSINMylan Pharmaceuticals Inc.6b887aa5-5edf-48c5-a480-dea8c35afa9d2022-01-20Warnings, Adverse reactionsExact identifier
rxcui: 197625
rxcui: 197626
rxcui: 197627
unii: 86P6PQK0MU
CarduraDOXAZOSINROERIGeefc47bc-c10f-49bb-8ef7-5999f798ab392022-01-20Warnings, Adverse reactionsExact identifier
rxcui: 197625
rxcui: 197626
rxcui: 197627
unii: 86P6PQK0MU
DoxazosinDOXAZOSINAphena Pharma Solutions - Tennessee, LLCf1dc70f6-4329-46da-8990-7bd6eec9d37d2021-12-07Warnings, Adverse reactionsExact identifier
application number: ANDA075580
rxcui: 197626
unii: 86P6PQK0MU
DoxazosinDOXAZOSIN MESYLATETeva Pharmaceuticals USA, Inc.0aaa68a7-f73b-46d8-860f-a76d968974892021-11-30Warnings, Adverse reactionsExact identifier
rxcui: 197625
rxcui: 197626
rxcui: 197627
unii: 86P6PQK0MU
DoxazosinDOXAZOSIN MESYLATEAphena Pharma Solutions - Tennessee, LLC6b74b18f-b89a-4109-a29e-c4fa65a3c5ee2020-12-10Warnings, Adverse reactionsExact identifier
rxcui: 197626
unii: 86P6PQK0MU
DoxazosinDOXAZOSINAphena Pharma Solutions - Tennessee, LLC7e547752-a53a-4ad9-b70e-7cc2a1dd5d5d2018-03-06Warnings, Adverse reactionsExact identifier
application number: ANDA075580
rxcui: 197627
unii: 86P6PQK0MU

Reported adverse events (FAERS/openFDA)#

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