FDA.reportPublic FDA data

NDC 50268-221-11 - 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
50268-221
Requested NDC
50268-221-11
Package NDCs from labels
50268-221-11, 50268-221-15
Manufacturer
AvPAK
Effective date
2022-01-25
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Desmopressin Acetate - AvPAKAvPAK2022-01-25HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50268-221-152022-01-31C16284748780-1d6a99b39-d179-a426-e053-dadaa90af4c2Desmopressin Acetate Tablets
50268-221-152022-01-28C16284748780-1d6a99b39-d179-a426-e053-dadaa90af4c2Desmopressin Acetate Tablets

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50268-221-11EA - Each50268-2215503b4fe-0f70-4ec2-ab53-78cef841727712015-04-03
50268-221-15EA - Each50268-221cf71ea87-61b4-46b2-9a73-58e2da4e848112013-10-17

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DESMOPRESSIN ACETATEACTIVE INGREDIENTXB13HYU18UDESMOPRESSIN ACETATE (DESMOPRESSIN ACETATE) TABLET [AVPAK]2
DESMOPRESSINACTIVE MOIETYENR1LLB0FPDESMOPRESSIN ACETATE (DESMOPRESSIN ACETATE) TABLET [AVPAK]2
BUTYLATED HYDROXYANISOLEINACTIVE INGREDIENTREK4960K2UDESMOPRESSIN ACETATE (DESMOPRESSIN ACETATE) TABLET [AVPAK]2
BUTYLATED HYDROXYTOLUENEINACTIVE INGREDIENT1P9D0Z171KDESMOPRESSIN ACETATE (DESMOPRESSIN ACETATE) TABLET [AVPAK]2
CROSPOVIDONEINACTIVE INGREDIENT68401960MKDESMOPRESSIN ACETATE (DESMOPRESSIN ACETATE) TABLET [AVPAK]2
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XDESMOPRESSIN ACETATE (DESMOPRESSIN ACETATE) TABLET [AVPAK]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30DESMOPRESSIN ACETATE (DESMOPRESSIN ACETATE) TABLET [AVPAK]2
POVIDONEINACTIVE INGREDIENTFZ989GH94EDESMOPRESSIN ACETATE (DESMOPRESSIN ACETATE) TABLET [AVPAK]2
STARCH, POTATOINACTIVE INGREDIENT8I089SAH3TDESMOPRESSIN ACETATE (DESMOPRESSIN ACETATE) TABLET [AVPAK]2

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 6 · 110 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Leader Artificial Tears 15 mLPOLYVINYL ALCOHOL, POVIDONECardinal Health8cccc589-3a8e-baad-e053-2a95a90ab8c72026-09-09WarningsExact identifier
unii: FZ989GH94E
FRESHKOTE PRESERVATIVE FREE LUBRICANT EYE DROPSPOVIDONE, POLYVINYL ALCOHOL SOLUTIONHarrow Eye, LLC049e9cc9-0663-53bc-e063-6294a90a2c4f2026-09-04WarningsExact identifier
unii: FZ989GH94E
Desmopressin AcetateDESMOPRESSIN ACETATEThe J. Molner Company LLC52680415-52a0-61c2-e063-6294a90ae27e2026-08-27Boxed warning, Warnings, Adverse reactionsExact identifier
unii: XB13HYU18U
Rohto Optic GlowNAPHAZOLINE HYDROCHLORIDE, POVIDONE, PROPYLENE GLYCOLThe Mentholatum Companydf9c5f7c-96e6-4b2b-b8cb-21a6a3342dff2026-08-20WarningsExact identifier
unii: FZ989GH94E
Rohto Preservative Free Dry AidPOVIDONE, PROPYLENE GLYCOLThe Mentholatum Companyf4b1974c-2412-45f6-b79d-88b8a0bcb6082026-08-18WarningsExact identifier
unii: FZ989GH94E
Rohto Dry-AidPOVIDONE, PROPYLENE GLYCOLThe Mentholatum Company8ea5c6c9-48f4-406a-a2cb-9280c546d87d2026-08-18WarningsExact identifier
unii: FZ989GH94E
GOOD NEIGHBOR PHARMACY ARTIFICAL TEARS LUBRICANT EYE DROPSPOLYVINYL ALCOHOL, POVIDONEAmerisourceBergence6852a8-c5e6-403d-a7b4-a2e85d1ebb1f2026-07-22WarningsExact identifier
unii: FZ989GH94E
StimateDESMOPRESSIN ACETATEFerring Pharmaceuticals Inc.f5ada39c-20ed-4500-9dce-1e4ab642a3582026-07-22Warnings, Adverse reactionsExact identifier
unii: XB13HYU18U
Desmopressin AcetateDESMOPRESSIN ACETATEArmas Pharmaceuticals Inc.d87168b9-f103-4ba5-b0b3-0656d1c81da22026-06-22Boxed warning, Warnings, Adverse reactionsExact identifier
unii: XB13HYU18U
Desmopressin AcetateDESMOPRESSIN ACETATEArmas Pharmaceuticals Inc.673cd9ab-b714-49ee-9ce7-c99be605c30e2026-06-19Boxed warning, Warnings, Adverse reactionsExact identifier
unii: XB13HYU18U
Rohto Sun and SportHYPROMELLOSE, POVIDONEThe Mentholatum Company8bcc8882-b886-4b55-9bc4-d4b92a41358f2026-06-19WarningsExact identifier
unii: FZ989GH94E
Rohto Dual Light ReliefHYPROMELLOSE, POVIDONEThe Mentholatum Company1b597f83-d7f1-cf93-e063-6394a90a99f72026-06-19WarningsExact identifier
unii: FZ989GH94E
RippleGLYCERIN, POVIDONECorneaCare Inc3b5ba197-d501-681e-e063-6294a90aefb52026-05-24WarningsExact identifier
unii: FZ989GH94E
iVIZIA Lubricant Eye GelPOVIDONEThea Pharma Inc.1f06ca1a-5270-9a82-e063-6294a90aed642026-04-29WarningsExact identifier
unii: FZ989GH94E
GoodSense Eye Drops Advanced Relief MoisturizerDEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCLPreferred PHarmaceuticals Inc.011473a8-26d5-4661-b3c0-745f9b6aa1d82026-04-29WarningsExact identifier
unii: FZ989GH94E
Desmopressin AcetateDESMOPRESSIN ACETATEREMEDYREPACK INC.f140926e-3201-4b8e-8207-14c560ddb55e2026-04-23Warnings, Adverse reactionsExact identifier
unii: XB13HYU18U
FreshKote Preservative Free Lubricant Eye DropsPOVIDONE, POLYVINYL ALCOHOLEyevance Pharmaceuticalsf51c50c3-43ae-4169-9d2b-22b239461dd12026-04-08WarningsExact identifier
unii: FZ989GH94E
Desmopressin AcetateDESMOPRESSIN ACETATECaplin Steriles Limited84dbb392-4535-4cbc-af60-75abb494f26e2026-03-16Boxed warning, Warnings, Adverse reactionsExact identifier
unii: XB13HYU18U
Leader Advanced Relief Eye DropsDEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCLCardinal Health5c5d6c13-9b51-48f0-8627-b60b0f707fd32026-03-12WarningsExact identifier
unii: FZ989GH94E
DESMODADESMOPRESSIN ACETATE ORAL SOLUTIONEton Pharmaceuticals, Inc.4c0e1356-d14f-cfb4-e063-6294a90acd272026-03-02Warnings, Adverse reactionsExact identifier
unii: XB13HYU18U

Reported adverse events (FAERS/openFDA)#

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