FDA.reportPublic FDA data

NDC 68084-604-11 - 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
68084-604
Requested NDC
68084-604-11
Package NDCs from labels
68084-604-11, 68084-604-21
Manufacturer
American Health Packaging
Effective date
2023-03-20
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Desmopressin Acetate - American Health PackagingAmerican Health Packaging2023-03-20HUMAN PRESCRIPTION DRUG LABEL
National Council for Prescription Drug Programs indexing - billing unitNational Council for Prescription Drug Programs2013-02-13Indexing - Billing Unit

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68084-604-11EA - Each68084-60407e9593c-eb20-4356-9097-50ed4b0e74e212013-02-13
68084-604-21EA - Each68084-604a3224d68-9c24-4db0-bb17-c91fd7b6b00112013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DESMOPRESSIN ACETATEACTIVE INGREDIENTXB13HYU18UDESMOPRESSIN ACETATE TABLET [AMERICAN HEALTH PACKAGING]3
DESMOPRESSINACTIVE MOIETYENR1LLB0FPDESMOPRESSIN ACETATE TABLET [AMERICAN HEALTH PACKAGING]3
BUTYLATED HYDROXYANISOLEINACTIVE INGREDIENTREK4960K2UDESMOPRESSIN ACETATE TABLET [AMERICAN HEALTH PACKAGING]3
BUTYLATED HYDROXYTOLUENEINACTIVE INGREDIENT1P9D0Z171KDESMOPRESSIN ACETATE TABLET [AMERICAN HEALTH PACKAGING]3
CROSPOVIDONEINACTIVE INGREDIENT68401960MKDESMOPRESSIN ACETATE TABLET [AMERICAN HEALTH PACKAGING]3
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XDESMOPRESSIN ACETATE TABLET [AMERICAN HEALTH PACKAGING]3
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30DESMOPRESSIN ACETATE TABLET [AMERICAN HEALTH PACKAGING]3
POVIDONESINACTIVE INGREDIENTFZ989GH94EDESMOPRESSIN ACETATE TABLET [AMERICAN HEALTH PACKAGING]3
STARCH, POTATOINACTIVE INGREDIENT8I089SAH3TDESMOPRESSIN ACETATE TABLET [AMERICAN HEALTH PACKAGING]3

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 6 · 108 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Harris Teeter Eye Drops Advanced ReliefDEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HYDROCHLORIDEHarris Teeter, LLCf76e2831-5c6c-7a62-e053-6294a90a937b2025-12-30WarningsExact identifier
unii: FZ989GH94E
CareOne Artificial Tears Eye Drops 15mLPOLYVINYL ALCOHOL, POVIDONERetail Business Services, LLC92fded6b-91fd-d82e-e053-2a95a90ab5232025-12-30WarningsExact identifier
unii: FZ989GH94E
Quality Choice Artificial Tears Lubricant Eye DropsPOLYVINYL ALCOHOL, POVIDONEChain Drug Marketing Association, Inc.1f669655-4bc7-0175-e063-6294a90a305a2025-12-30WarningsExact identifier
unii: FZ989GH94E
Equate Artificial TearsPOLYVINYL ALCOHOL, POVIDONEWalmart, Inc.ead9f271-0f15-1fff-e053-2a95a90a93ac2025-12-30WarningsExact identifier
unii: FZ989GH94E
Eye Love Heyedrate Long Lasting HydrationGLYCERIN, POVIDONEPhysician Recommended Neutraceuticals, L.P.f321dea1-3251-eaa8-e053-2995a90aaf952025-12-30WarningsExact identifier
unii: FZ989GH94E
Quality Choice Moisturizing Relief Eye DropsDEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCLChain Drug Marketing Association, Inc.1fb81759-5931-59c8-e063-6294a90a22772025-12-30WarningsExact identifier
unii: FZ989GH94E
Desmopressin AcetateDESMOPRESSIN ACETATEAmerican Health Packaging0d447b48-3f4b-430e-9e68-d8b9401c002e2025-11-13Warnings, Adverse reactionsExact identifier
unii: XB13HYU18U
Desmopressin AcetateDESMOPRESSIN ACETATEBryant Ranch Prepackdc9b0dad-d265-4dff-8191-d936280d85a22025-11-07Warnings, Adverse reactionsExact identifier
unii: XB13HYU18U
LACRIFRESH HYDRAPFGLYCERIN, POVIDONEAVIZOR, S.A.41bbd23e-0ec8-eb18-e063-6294a90a46d12025-10-27WarningsExact identifier
unii: FZ989GH94E
LACRIFRESH HYDRAMAXPFGLYCERIN, POVIDONEAVIZOR, S.A.41be1604-89b4-7ec3-e063-6294a90a33312025-10-27WarningsExact identifier
unii: FZ989GH94E
Desmopressin AcetateDESMOPRESSIN ACETATENordic Pharma, Inc.29df0492-f7ef-47bb-aa67-4ef9e5c2846f2025-10-24Boxed warning, Warnings, Adverse reactionsExact identifier
unii: XB13HYU18U
StyePOLYVINYL ALCOHOL AND POVIDONEMedtech Products Inc.60c11d3d-df20-4d1c-b425-49a84fecea302025-10-23WarningsExact identifier
unii: FZ989GH94E
Desmopressin AcetateDESMOPRESSIN ACETATENordic Pharma, Inc.10b29aa2-274e-4c29-bccd-424bd37617582025-10-23Boxed warning, Warnings, Adverse reactionsExact identifier
unii: XB13HYU18U
iVIZIA Dry EyePOVIDONEThea Pharma Inc.1ef73cb1-da48-a713-e063-6294a90afa9d2025-10-20WarningsExact identifier
unii: FZ989GH94E
Eyes Irritation ReliefPOLYVINYL ALCOHOL AND POVIDONE AND TETRAHYDROZOLINE HYDROCHLORIDECARDINAL HEALTH 110, LLC. DBA LEADERbd2608c6-ffdf-352a-e053-2995a90a26a82025-09-12WarningsExact identifier
unii: FZ989GH94E
Desmopressin AcetateDESMOPRESSIN ACETATENordic Pharma, Inc.131fd4d8-48ca-4c1f-8165-848dc0a4d5112025-07-23Boxed warning, Warnings, Adverse reactionsExact identifier
unii: XB13HYU18U
Desmopressin AcetateDESMOPRESSIN ACETATEOceanside Pharmaceuticals8034989a-45f5-436b-8b1f-42108ee2a21a2025-06-19Warnings, Adverse reactionsExact identifier
unii: XB13HYU18U
DESMOPRESSIN ACETATEDESMOPRESSIN ACETATEUBI Pharma Inc.b01c22dc-eecd-11b2-e053-2a95a90a529a2025-02-19Boxed warning, Warnings, Adverse reactionsExact identifier
unii: XB13HYU18U
Walgreens Soothing Eye Relief Lubricant Eye DropsPOLYVINYL ALCOHOL, POVIDONEWalgreens Co.29b7387b-ad65-3a11-e063-6394a90a6a152025-02-14WarningsExact identifier
unii: FZ989GH94E
Desmopressin AcetateDESMOPRESSIN ACETATEBryant Ranch Prepack52133714-37d1-458d-9839-f0bd206711ea2025-01-31Warnings, Adverse reactionsExact identifier
unii: XB13HYU18U

Reported adverse events (FAERS/openFDA)#

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