NDC 70710-1238-01 - 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
70710-1238
Requested NDC
70710-1238-01
Package NDCs from labels
70710-1238-1, 70710-1238-01
Manufacturer
Zydus Pharmaceuticals (USA) Inc. | Zydus Lifesciences Global FZE | Zydus Lifesciences Limited
Effective date
2024-03-26
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
acetaZOLAMIDE Tablets, USP RX OnlyZydus Pharmaceuticals (USA) Inc. | Zydus Lifesciences Global FZE | Zydus Lifesciences Limited2024-03-26HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70710-1238-1acetaZOLAMIDE100 in 1 BOTTLETABLET1003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70710-1238ACETAZOLAMIDE TABLET [ZYDUS PHARMACEUTICALS (USA) INC.]3Current NDC, 1 package rows20240328_85e4d8f6-1e82-4068-a768-752287d4ccf2.zip

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 3 of 3 · 51 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AcetazolamideACETAZOLAMIDEChartwell RX, LLCf75bbf55-98ac-4f91-b6fd-17b5ac860e552024-10-10Warnings, Adverse reactionsExact identifier
rxcui: 197303
rxcui: 197304
unii: O3FX965V0I
acetazolamideACETAZOLAMIDEZydus Pharmaceuticals (USA) Inc.bf514e99-4958-44a0-a87a-02a950f87e602024-10-08Warnings, Adverse reactionsExact identifier
unii: O3FX965V0I
acetazolamideACETAZOLAMIDEZydus Lifesciences Limited2c1d9078-c15f-4dce-bc26-edfa5400fa9b2024-10-08Warnings, Adverse reactionsExact identifier
unii: O3FX965V0I
AcetazolamideACETAZOLAMIDEAlembic Pharmaceuticals Inc.43231abb-2a5d-44ab-b3e6-7564a1131ac52024-09-30Warnings, Adverse reactionsExact identifier
unii: O3FX965V0I
acetaZOLAMIDEACETAZOLAMIDENuCare Pharmaceuticals,Inc.1b2c973f-82ef-a4f3-e063-6394a90aaae02024-08-09Warnings, Adverse reactionsExact identifier
application number: ANDA211069
rxcui: 197303
unii: O3FX965V0I
acetaZOLAMIDEACETAZOLAMIDEZydus Pharmaceuticals (USA) Inc.85e4d8f6-1e82-4068-a768-752287d4ccf22024-03-26Warnings, Adverse reactionsExact identifier
application number: ANDA211069
ndc (package): 70710-1239-1
ndc (package): 70710-1238-1
ndc (product): 70710-1238
ndc (product): 70710-1239
ndc11 (package): 70710123801
rxcui: 197303
rxcui: 197304
spl id: b8ec300c-c64c-4a65-a101-66644f64f9f7
spl set id: 85e4d8f6-1e82-4068-a768-752287d4ccf2
unii: O3FX965V0I
Pure Cornstarch BabyCORN STARCHWalgreen Companyd0e9bd13-b568-4f7e-b036-8d23e71ad8bf2024-03-25WarningsExact identifier
unii: O8232NY3SJ
ACETAZOLAMIDE EXTENDED-RELEASEACETAZOLAMIDE EXTENDED-RELEASEAvPAKe43f991d-15b9-1e66-e053-2a95a90a94492024-01-09Warnings, Adverse reactionsExact identifier
unii: O3FX965V0I
ACETAZOLAMIDEACETAZOLAMIDETRUPHARMA, LLC4fcd428a-7bf3-4e75-a834-1bdf1078107f2022-06-13Warnings, Adverse reactionsExact identifier
rxcui: 197303
rxcui: 197304
unii: O3FX965V0I
AcetazolamideACETAZOLAMIDEProficient Rx LP3cdde6aa-c89d-4ea4-aade-6c8b5c3ffdcc2019-10-01Warnings, Adverse reactionsExact identifier
rxcui: 197303
unii: O3FX965V0I
AcetazolamideACETAZOLAMIDEAlembic Pharmaceuticals Limitedd9c1cc75-4e3d-4eaf-87c5-d5942a8438182019-02-20Warnings, Adverse reactionsExact identifier
unii: O3FX965V0I

Reported adverse events (FAERS/openFDA)#

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