NDC 70436-190-80 - Esomeprazole 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: 70436-190
Requested NDC: 70436-190-80
Package NDCs from labels: 70436-190-80, 70436-190-82
Manufacturer: Slate Run Pharmaceuticals, LLC | Hainan Poly Pharm. Co., Ltd.
Effective date: 2026-06-22
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
EDETATE DISODIUM - Slate Run Pharmaceuticals, LLC \| Hainan Poly Pharm. Co., Ltd.	Slate Run Pharmaceuticals, LLC \| Hainan Poly Pharm. Co., Ltd.	2026-06-22	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70436-190-80	Esomeprazole sodium	5 mL in 1 VIAL	INJECTION, POWDER, LYOPHILIZED,	5		3
70436-190-82	Esomeprazole sodium	10 in 1 CARTON	INJECTION, POWDER, LYOPHILIZED,	10		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70436-190	ESOMEPRAZOLE SODIUM INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [SLATE RUN PHARMACEUTICALS, LLC]	3	Current NDC, Legacy NDC, 2 package rows	20231026_23395673-116d-4a8e-b0ce-59f9ca5b3daf.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
70436-190-80	EA - Each	70436-190	69bd9588-e20e-4090-98ef-e631c2777fa2	1	2022-06-06
70436-190-82	EA - Each	70436-190	f6cc5601-5ca2-40a6-806d-3c0f609ae3cf	1	2022-06-06

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 1 of 1 · 5 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Esomeprazole sodium	ESOMEPRAZOLE SODIUM	Slate Run Pharmaceuticals, LLC	23395673-116d-4a8e-b0ce-59f9ca5b3daf	2026-06-22	Warnings, Adverse reactions	Exact identifier application number: ANDA215732 ndc (package): 70436-190-80 ndc (package): 70436-190-82 ndc (product): 70436-190 ndc11 (package): 70436019080 rxcui: 486501 spl id: 54e3fe0f-b6a6-6b5d-e063-6294a90a836a spl set id: 23395673-116d-4a8e-b0ce-59f9ca5b3daf unii: L2C9GWQ43H
Esomeprazole Sodium	ESOMEPRAZOLE SODIUM	Eugia US LLC	45a15ba2-2aae-4edc-beaa-4a2357d87f32	2025-11-07	Warnings, Adverse reactions	Exact identifier rxcui: 486501 unii: L2C9GWQ43H
Esomeprazole Sodium	ESOMEPRAZOLE SODIUM	Gland Pharma Limited	9354958c-e997-41c8-8605-23f0a58993c0	2023-07-21	Warnings, Adverse reactions	Exact identifier rxcui: 486501 unii: L2C9GWQ43H
Miracle FootCream Lavender	UREA, GLYCERIN, ALOE, DISODIUM EDTA	Aloe Vera Korea Co.,Ltd.	db520c80-2a2a-5eb1-e053-2995a90a5bb4	2022-03-28	Warnings	Exact identifier unii: 7FLD91C86K
Miracle FootCream Lemon	UREA, GLYCERIN, ALOE, DISODIUM EDTA	Aloe Vera Korea Co.,Ltd.	db525c63-29fd-2033-e053-2995a90a56b9	2022-03-28	Warnings	Exact identifier unii: 7FLD91C86K

Reported adverse events (FAERS/openFDA)#

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