NDC 70518-4612-01 - Desmopressin Acetate

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
70518-4612
Requested NDC
70518-4612-01
Package NDCs from labels
70518-4612-1, 70518-4612-0, 70518-4612-01
Manufacturer
REMEDYREPACK INC.
Effective date
2026-04-23
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Desmopressin Acetate Tablets Rx onlyREMEDYREPACK INC.2026-04-23HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-4612-0Desmopressin Acetate50 in 1 BOXTABLET501
70518-4612-1Desmopressin Acetate1 in 1 POUCHTABLET11

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 · 45 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Desmopressin AcetateDESMOPRESSIN ACETATEBauch & Lomb Incorporated8ca799f1-7029-4527-9ab4-7512504bb8e22021-09-01Warnings, Adverse reactionsExact identifier
unii: XB13HYU18U
DDAVPDESMOPRESSIN ACETATEFerring Pharmaceuticals Inc.6d55baa9-2b62-469c-93ae-3909ab2493322021-02-03Warnings, Adverse reactionsExact identifier
rxcui: 833008
rxcui: 849515
unii: XB13HYU18U
desmopressin acetateDESMOPRESSIN ACETATESun Pharmaceutical Industries, Inc.2dc2cec8-6953-4a33-9356-11534fba1fb82020-01-23Warnings, Adverse reactionsExact identifier
unii: XB13HYU18U
DESMOPRESSIN ACETATEDESMOPRESSIN ACETATEDr.Reddys' Laboratories Inc15179e0c-f677-307f-d1e1-5910de4c212f2019-11-30Warnings, Adverse reactionsExact identifier
unii: XB13HYU18U
Desmopressin AcetateDESMOPRESSIN ACETATEGlenmark Pharmaceuticals Inc.,USA7a26b415-77cd-4b2f-9c76-fa52d2eb6be62019-06-28Warnings, Adverse reactionsExact identifier
rxcui: 833008
rxcui: 849515
unii: XB13HYU18U

Reported adverse events (FAERS/openFDA)#

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