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 88 of 280 · 5,597 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Isopropyl Alcohol 50%ISOPROPYL ALCOHOL 50%Hydrox Laboratories930bb3a3-5ca3-414c-b4fb-c71ee17fc7462026-01-12WarningsExact identifier
unii: ND2M416302
Instant Hand SanitizerALCOHOLHydrox Laboratoriesa818def4-f6e9-4a97-aa26-b7c082ae8d182026-01-12WarningsExact identifier
unii: 3K9958V90M
Instant Hand SanitizerALCOHOLHydrox Laboratories285505b0-ee49-4d01-9019-1052e2fb19642026-01-12WarningsExact identifier
unii: 3K9958V90M
Isopropyl AlcoholISOPROPYL ALCOHOLHydrox Laboratoriesf2f07464-6bd5-434c-8dea-0ba659c0e5492026-01-12WarningsExact identifier
unii: ND2M416302
Instant Hand Sanitizer UnscentedALCOHOLHydrox Laboratoriescd42da2c-0235-4410-945b-baabb5c7931b2026-01-12WarningsExact identifier
unii: 3K9958V90M
Isopropyl Alcohol with Wintergreen 70%ISOPROPYL ALCOHOL WITH WINTERGREEN 70%Hydrox Laboratories5845f723-8866-4738-bec6-621041899f572026-01-12WarningsExact identifier
unii: ND2M416302
Isopropyl AlcoholISOPROPYL ALCOHOLHydrox Laboratories2042cf29-52c5-4f1e-aae6-78e025994d182026-01-12WarningsExact identifier
unii: ND2M416302
Isopropyl Alcohol with Wintergreen 50%ISOPROPYL ALCOHOL WITH WINTERGREEN 50%Hydrox Laboratories3a15a900-2b48-487f-b252-a1a1e0d0abfc2026-01-12WarningsExact identifier
unii: ND2M416302
Instant Hand SanitizerALCOHOLLTC Products Inc.6c16aeec-bef2-41f1-b22d-ac37c36255622026-01-12WarningsExact identifier
unii: 3K9958V90M
Isopropyl Rubbing AlcoholISOPROPYL ALCOHOLDiscount Drug Mart37a6c0fb-e9c4-4a95-9539-ca5766b3a7012026-01-12WarningsExact identifier
unii: ND2M416302
Isopropyl AlcoholISOPROPYL ALCOHOLDiscount Drug Mart7ac6b062-b471-4653-9d6f-de2ca8f8b0142026-01-12WarningsExact identifier
unii: ND2M416302
Isopropyl Rubbing AlcoholISOPROPYL ALCOHOLEpic Medical Supply Corp.88e6418c-ceb3-4bd6-8765-b476d8bf3ff32026-01-12WarningsExact identifier
unii: ND2M416302
Blue Lizard Sensitive SPF 50 SunscreenTITANIUM DIOXIDE AND ZINC OXIDECrown Laboratories9d20b230-2cce-4d90-e053-2995a90a4c032026-01-12WarningsExact identifier
unii: 15FIX9V2JP
Blue Lizard Sheer SPF 50 SunscreenTITANIUM DIOXIDE, ZINC OXIDECrown Laboratoriesc20fce25-8120-fe5d-e053-2a95a90a53a02026-01-12WarningsExact identifier
unii: 15FIX9V2JP
Blue Lizard Sheer Face SPF 50 SunscreenTITANIUM DIOXIDE AND ZINC OXIDECrown Laboratoriesbaed8202-21fd-3a43-e053-2a95a90ada322026-01-12WarningsExact identifier
unii: 15FIX9V2JP
Blue Lizard Sensitive Face SunscreenTITANIUM DIOXIDE, ZINC OXIDECrown Laboratories88dbd396-8955-271e-e053-2995a90a0a7a2026-01-12WarningsExact identifier
unii: 15FIX9V2JP
Hand Essentials Instant Hand AntisepticETHYL ALCOHOLHu-Friedy Mfg. Co., Inc.a580ebfb-2da9-4a20-9a3c-6244dbb7aef12026-01-12WarningsExact identifier
unii: 3K9958V90M
Blue Lizard Baby SPF 50 SunscreenTITANIUM DIOXIDE AND ZINC OXIDECrown Laboratories9d237fb7-4f5f-521d-e053-2a95a90a97342026-01-12WarningsExact identifier
unii: 15FIX9V2JP
Epi-Clenz Pure Instant Hand AntisepticETHYL ALCOHOLMedline Industries, LP9f2be060-0699-47ab-9398-efe91eef22672026-01-12WarningsExact identifier
unii: 3K9958V90M
Blue Lizard Sensitive SunscreenTITANIUM DIOXIDE AND ZINC OXIDECrown Laboratories1e4d49f4-9e77-48b5-bce5-ff04ed885a0f2026-01-12WarningsExact identifier
unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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