FDA.reportPublic FDA data

NDC 70095-024-01 - Pantoprazole sodium

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
70095-024
Requested NDC
70095-024-01
Package NDCs from labels
70095-024-01, 70095-024-02, 70095-024-03
Manufacturer
Sun Pharmaceutical Industries Limited | Gland Pharma Limited
Effective date
2025-04-01
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
PANTOPRAZOLE - Sun Pharmaceutical Industries Limited | Gland Pharma LimitedSun Pharmaceutical Industries Limited | Gland Pharma Limited2025-04-01Human Prescription Drug Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70095-024-01Pantoprazole sodium10 mL in 1 VIALINJECTION, POWDER, LYOPHILIZED,104
70095-024-02Pantoprazole sodium1 in 1 CARTONINJECTION, POWDER, LYOPHILIZED,14
70095-024-02Pantoprazole sodium10 in 1 PACKAGEINJECTION, POWDER, LYOPHILIZED,104
70095-024-03Pantoprazole sodium25 in 1 PACKAGEINJECTION, POWDER, LYOPHILIZED,254
70095-024-03Pantoprazole sodium1 in 1 CARTONINJECTION, POWDER, LYOPHILIZED,14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70095-024PANTOPRAZOLE SODIUM INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [SUN PHARMACEUTICAL INDUSTRIES LIMITED]4Current NDC, 5 package rows20250406_eb3f58d4-0c69-4377-be45-c36099c98d33.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70095-024-01EA - Each70095-0242ed3b743-c98b-4188-bd77-39799db3875d12023-07-06
70095-024-02EA - Each70095-024a764b9eb-0f5e-42bf-bff9-eca33ea55f4812023-06-06
70095-024-03EA - Each70095-0247ad39138-1b02-42d1-880c-96ee7da1476712023-06-06

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 7 · 138 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PantoprazolePANTOPRAZOLEPHOENIX RX LLC43fc6326-cfe6-7d1c-e063-6394a90abc242025-11-19Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
Pantoprazole SodiumPANTOPRAZOLE SODIUMCardinal Health 107, LLC4ba4c797-3f97-4d85-971e-7b17bdf892212025-11-06Warnings, Adverse reactionsExact identifier
rxcui: 283669
unii: 6871619Q5X
PantoprazolePANTOPRAZOLEAdvanced Rx of Tennessee, LLC4136d983-75fa-9604-e063-6294a90aaac62025-10-15Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
Pantoprazole SodiumPANTOPRAZOLE SODIUMCardinal Health 107, LLC362229c5-7b28-4563-aa62-d97d060054802025-10-13Warnings, Adverse reactionsExact identifier
rxcui: 283669
unii: 6871619Q5X
PANTOPRAZOLE SODIUM I.V.PANTOPRAZOLE SODIUMPiramal Critical Care0696b10c-972b-9dcf-e063-6294a90a10342025-10-07Warnings, Adverse reactionsExact identifier
rxcui: 283669
unii: 6871619Q5X
Pantoprazole SodiumPANTOPRAZOLE SODIUMPD-Rx Pharmaceuticals, Inc.b422c5eb-9a6d-4f8c-863d-ca515ec780c22025-10-02Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
Pantoprazole SodiumPANTOPRAZOLEBryant Ranch Prepackd212e8ec-f7ff-4727-a83e-0edc4ca7e6d12025-09-26Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
Pantoprazole sodium delayed-releasePANTOPRAZOLE SODIUM DELAYED-RELEASELifestar Pharma LLC0502f935-af7a-4f1e-8c3e-29e20647c8852025-09-08Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
PANTOPRAZOLE SODIUM I.V.PANTOPRAZOLE SODIUMSandoz Inc22b71a1d-87f8-43ba-b53d-53ca3f70c63e2025-07-30Warnings, Adverse reactionsExact identifier
rxcui: 283669
unii: 6871619Q5X
Pantoprazole SodiumPANTOPRAZOLE SODIUMDevatis Inc.13c337e7-1e7b-47bd-9f88-92b0d548ca9c2025-07-30Warnings, Adverse reactionsExact identifier
rxcui: 283669
unii: 6871619Q5X
Pantoprazole SodiumPANTOPRAZOLE SODIUMMylan Institutional Inc.a9b0d279-118b-4372-bd51-d4bad9c1cfca2025-07-22Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
Pantoprazole SodiumPANTOPRAZOLE SODIUMMeitheal Pharmaceuticals Inc.014f9762-6948-46b7-8659-5c89f35ad8bf2025-06-27Warnings, Adverse reactionsExact identifier
rxcui: 283669
unii: 6871619Q5X
Pantoprazole SodiumPANTOPRAZOLE SODIUMAphena Pharma Solutions - Tennessee, LLCc9bc288b-e84c-4e31-a769-c87a592260862025-06-09Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
Protonix I.V.PANTOPRAZOLE SODIUMCardinal Health 107, LLC3cde88e6-28f2-4cbe-8c3f-770b05cc0e1b2025-04-22Warnings, Adverse reactionsExact identifier
rxcui: 283669
unii: 6871619Q5X
PANTOPRAZOLE SODIUMPANTOPRAZOLE SODIUM INJECTIONAlembic Pharmaceuticals Limited02ee7ed6-217f-4128-bbbb-b9390475a65b2025-04-07Warnings, Adverse reactionsExact identifier
rxcui: 283669
unii: 6871619Q5X
PANTOPRAZOLE SODIUMPANTOPRAZOLE SODIUM INJECTIONAlembic Pharmaceuticals Inc.a9e5fac6-2db6-4311-a98b-eb3f0dde19d62025-04-07Warnings, Adverse reactionsExact identifier
rxcui: 283669
unii: 6871619Q5X
PANTOPRAZOLE SODIUMPANTOPRAZOLE SODIUMRising Pharma Holdings, Inc.91a6b13f-457f-4136-9541-c4adb9c3c35c2025-04-02Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
PANTOPRAZOLE SODIUMPANTOPRAZOLE SODIUMAurobindo Pharma Limitedb3cec41e-e98b-470a-8ba2-c315370239892025-04-02Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
PANTOPRAZOLE SODIUM DELAYED-RELEASE delayed releasePANTOPRAZOLE SODIUM GRANULESCipla USA Inc.195e06db-b76c-4470-b6a5-a3979c25046d2025-04-01Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
Pantoprazole sodiumPANTOPRAZOLE SODIUMSun Pharmaceutical Industries Limitedeb3f58d4-0c69-4377-be45-c36099c98d332025-04-01Warnings, Adverse reactionsExact identifier
application number: ANDA204400
ndc (package): 70095-024-03
ndc (package): 70095-024-02
ndc (package): 70095-024-01
ndc (product): 70095-024
ndc11 (package): 70095002401
rxcui: 283669
spl id: b423abbc-01e1-4d07-9c89-a7398c898d2f
spl set id: eb3f58d4-0c69-4377-be45-c36099c98d33
unii: 6871619Q5X

Reported adverse events (FAERS/openFDA)#

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