FDA.reportPublic FDA data

NDC 71288-600-91 - 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
71288-600
Requested NDC
71288-600-91
Package NDCs from labels
71288-600-91, 71288-600-92, 71288-600-10, 71288-600-11
Manufacturer
Meitheal Pharmaceuticals Inc. | Nanjing King-Friend Biochemical Pharmaceutical Co., Ltd.
Effective date
2025-06-27
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Pantoprazole SodiumMeitheal Pharmaceuticals Inc. | Nanjing King-Friend Biochemical Pharmaceutical Co., Ltd.2025-06-27HUMAN PRESCRIPTION DRUG LABEL
Pantoprazole SodiumMeitheal Pharmaceuticals Inc. | Nanjing King-Friend Biochemical Pharmaceutical Co., Ltd.2025-03-13HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71288-600-10Pantoprazole Sodium10 mL in 1 VIAL, SINGLE-DOSEINJECTION, POWDER, FOR SOLUTION106
71288-600-11Pantoprazole Sodium10 in 1 CARTONINJECTION, POWDER, FOR SOLUTION106
71288-600-91Pantoprazole Sodium10 mL in 1 VIAL, SINGLE-DOSEINJECTION, POWDER, FOR SOLUTION101
71288-600-92Pantoprazole Sodium10 in 1 CARTONINJECTION, POWDER, FOR SOLUTION101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71288-600PANTOPRAZOLE SODIUM INJECTION, POWDER, FOR SOLUTION [MEITHEAL PHARMACEUTICALS INC.]6Current NDC, Legacy NDC, 2 package rows20250514_c18aff31-f91e-4b6a-9713-52c9094c6082.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71288-600-10EA - Each71288-60051d04097-e4b5-4699-baf2-a6e6be97ecac12023-04-07
71288-600-11EA - Each71288-6007d126adc-cb4c-4b7d-8814-1d270690ff3e12023-04-07

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 7 of 7 · 138 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Pantoprazole SodiumPANTOPRAZOLE SODIUMCamber Pharmaceuticals, Inc.ee6278c0-d8c0-417c-a65c-b522ff76fe442023-11-02Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
PantoprazolePANTOPRAZOLEDr.Reddy's Laboratories Limited564709e8-358f-c185-4ecb-b3849c3fe59c2023-08-30Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
Pantoprazole SodiumPANTOPRAZOLE SODIUMMylan Pharmaceuticals Inc.56ad5b97-8e5f-48a5-b2ba-a5484b43d0182023-08-15Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
PANTOPRAZOLE SODIUMPANTOPRAZOLE SODIUMSun Pharmaceutical Industries, Inc.38353b9e-63bd-47e8-b7cb-b198d1e901f92023-08-03Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
Pantoprazole SodiumPANTOPRAZOLE SODIUMA-S Medication Solutionsf1eb666a-120d-47fd-8c9f-73cef839294a2023-07-31Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
Pantoprazole SodiumPANTOPRAZOLE SODIUMLannett Company, Inc.e7705bf6-e473-4b9c-bb5d-57e26ffe7b972023-07-21Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
Pantoprazole SodiumPANTOPRAZOLE SODIUMHikma Pharmaceuticals USA Inc.1e102c44-232b-4aaf-b457-2a740c47193a2023-07-19Warnings, Adverse reactionsExact identifier
rxcui: 283669
unii: 6871619Q5X
Pantoprazole SodiumPANTOPRAZOLE SODIUMHikma Pharmaceuticals USA Inc.b02f3f85-8f9b-4d06-8eae-73e592626f3e2023-07-10Warnings, Adverse reactionsExact identifier
rxcui: 283669
unii: 6871619Q5X
PANTOPRAZOLE SODIUMPANTOPRAZOLEAphena Pharma Solutions - Tennessee, LLCc10e9c12-e39d-4b0b-bd4c-10d3e9a4cf342023-02-17Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
PANTOPRAZOLE SODIUMPANTOPRAZOLEXLCare Pharmaceuticals Inc.17468dbf-84b6-4c53-9ad5-341350d2cfab2023-01-17Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
PANTOPRAZOLE SODIUMPANTOPRAZOLEAphena Pharma Solutions - Tennessee, LLCe3f711d8-b9d3-46a6-8bf9-6af1cc77003e2022-07-15Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
Pantoprazole SodiumPANTOPRAZOLE SODIUMProficient Rx LPa03aa46f-9eb5-4cf4-addf-745d94af82612022-06-01Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
Pantoprazole SodiumPANTOPRAZOLEProficient Rx LPa7dc4321-331d-49af-976c-cfd69d0055d92022-05-02Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
Miracle FootCream LavenderUREA, GLYCERIN, ALOE, DISODIUM EDTAAloe Vera Korea Co.,Ltd.db520c80-2a2a-5eb1-e053-2995a90a5bb42022-03-28WarningsExact identifier
unii: 7FLD91C86K
Miracle FootCream LemonUREA, GLYCERIN, ALOE, DISODIUM EDTAAloe Vera Korea Co.,Ltd.db525c63-29fd-2033-e053-2995a90a56b92022-03-28WarningsExact identifier
unii: 7FLD91C86K
Pantoprazole SodiumPANTOPRAZOLE SODIUMNovadoz Pharmaceuticals LLC1172bc4e-1700-402f-8262-97f05bac0d092022-03-03Warnings, Adverse reactionsExact identifier
rxcui: 283669
unii: 6871619Q5X
PANTOPRAZOLE SODIUMPANTOPRAZOLEProficient Rx LPdce2e97a-cd92-46b9-9444-91739bdcd5262019-11-01Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X
Pantoprazole SodiumPANTOPRAZOLEProficient Rx LP6d03491f-20c6-4878-9741-2e21e221eff22019-11-01Warnings, Adverse reactionsExact identifier
unii: 6871619Q5X

Reported adverse events (FAERS/openFDA)#

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