NDC 70710-1591-01 - acetazolamide

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
70710-1591
Requested NDC
70710-1591-01
Package NDCs from labels
70710-1591-3, 70710-1591-9, 70710-1591-1, 70710-1591-5, 70710-1591-0, 70710-1591-4, 70710-1591-01
Manufacturer
American Health Packaging
Effective date
2025-05-30
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
acetazolamide - American Health PackagingAmerican Health Packaging2025-05-30HUMAN PRESCRIPTION DRUG LABEL
acetazolamide - Zydus Pharmaceuticals (USA) Inc. | Zydus Lifesciences LimitedZydus Pharmaceuticals (USA) Inc. | Zydus Lifesciences Limited2024-10-08HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70710-1591-0acetazolamide1000 in 1 BOTTLECAPSULE10008
70710-1591-1acetazolamide100 in 1 BOTTLECAPSULE1008
70710-1591-3acetazolamide30 in 1 BOTTLECAPSULE308
70710-1591-4acetazolamide10 in 1 BLISTER PACKCAPSULE108
70710-1591-4acetazolamide10 in 1 CARTONCAPSULE108
70710-1591-5acetazolamide500 in 1 BOTTLECAPSULE5008
70710-1591-9acetazolamide90 in 1 BOTTLECAPSULE908

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70710-1591ACETAZOLAMIDE CAPSULE [ZYDUS PHARMACEUTICALS (USA) INC.]8Current NDC, Legacy NDC, 7 package rows20241012_bf514e99-4958-44a0-a87a-02a950f87e60.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70710-1591-1EA - Each70710-159155671302-c3bc-46f9-8d04-26bde539c17012020-04-20

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 218 of 273 · 5,447 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MistALCOHOLDerma Glove7c21ee1c-ce2a-464b-8269-cdb3e59db0942024-10-09WarningsExact identifier
unii: 3K9958V90M
HandLOTIONDerma Glovebcd71f37-63aa-4ad9-a9be-e5519c7e66e72024-10-09WarningsExact identifier
unii: 3K9958V90M
Hand ReliefLOTIONDerma Gloveffdfb167-0efa-4cd8-afdf-e1ff69ee62522024-10-09WarningsExact identifier
unii: 3K9958V90M
MistALCOHOLDerma Glove11c2939c-e77a-48f6-949c-9d508714012b2024-10-09WarningsExact identifier
unii: 3K9958V90M
Hand RecoveryALCOHOLDerma Glovee6cfe092-cb2c-441b-8897-98626c43bef82024-10-09WarningsExact identifier
unii: 3K9958V90M
HandLOTIONDerma Glove642cc56f-9f39-46be-bbd8-a2346a0efac42024-10-09WarningsExact identifier
unii: 3K9958V90M
HandLOTIONDerma Glove93736944-7535-4035-93aa-4771138af8e32024-10-09WarningsExact identifier
unii: 3K9958V90M
Hand ReliefLOTIONDerma Glove39867f66-b641-4060-881d-161c2591d19c2024-10-09WarningsExact identifier
unii: 3K9958V90M
Hand ReliefLOTIONDerma Glove767cc1f2-89a2-4d0b-ae49-ad7b9afca18b2024-10-09WarningsExact identifier
unii: 3K9958V90M
Hand RecoveryALCOHOLDerma Gloveb4ff67d6-27d6-4d31-a708-9c2e8d4f0f3e2024-10-09WarningsExact identifier
unii: 3K9958V90M
HandLOTIONDerma Glove1c46e4da-7594-48b0-8e8d-8031891184202024-10-09WarningsExact identifier
unii: 3K9958V90M
Hand SanitizerHAND SANITIZER UNSCENTEDCASAD Company, Inc07a891a3-dcf7-438f-bbf7-a20b2aa7d7d72024-10-09WarningsExact identifier
unii: 3K9958V90M
MistALCOHOLDerma Glovedd849fb3-95af-4a32-9687-3b966d456fbb2024-10-09WarningsExact identifier
unii: 3K9958V90M
Hand SanitizerHAND SANITIZER UNSCENTEDCASAD Company, Inc0933de73-94b1-448e-b39f-ecffabf952882024-10-09WarningsExact identifier
unii: 3K9958V90M
Hand RecoveryALCOHOLDerma Gloved8705086-7209-4f13-bd54-604c90495f0a2024-10-09WarningsExact identifier
unii: 3K9958V90M
HandLOTIONDerma Gloved158394e-baec-4770-8ee8-19285722ca612024-10-09WarningsExact identifier
unii: 3K9958V90M
AMOREPACIFIC COLOR CONTROL CUSHION COMPACT NO.102ZINC OXIDE, OCTINOXATE, AND TITANIUM DIOXIDEAMOREPACIFIC CORPORATION531f60c9-c89a-46bc-8460-d01b2e838e6f2024-10-08WarningsExact identifier
unii: 15FIX9V2JP
AMOREPACIFIC COLOR CONTROL CUSHION COMPACT NO.104OCTINOXATE, TITANIUM DIOXIDE, AND ZINC OXIDEAMOREPACIFIC CORPORATION60964d9f-d96c-4397-b273-6b63d18867222024-10-08WarningsExact identifier
unii: 15FIX9V2JP
IOPE AIR CUSHION Cover 21 VanillaZINC OXIDE, OCTINOXATE, AND TITANIUM DIOXIDEAMOREPACIFIC CORPORATION29d6cc8d-1469-479d-a15a-e78d4e22d4a22024-10-08WarningsExact identifier
unii: 15FIX9V2JP
FOAMING HAND ALCOHOL FOAMALCOHOLDraco Hygienic Products Inc.14860a19-e1e8-71fc-e063-6394a90a9df82024-10-08WarningsExact identifier
unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

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