FDA.reportPublic FDA data

NDC 76299-321-01 - Stendra

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
76299-321
Requested NDC
76299-321-01
Package NDCs from labels
76299-321-01, 76299-321-96, 76299-321-85, 76299-321-88
Manufacturer
Mist Pharmaceuticals, LLC
Effective date
2021-05-24
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Stendra - Mist Pharmaceuticals, LLCMist Pharmaceuticals, LLC2021-05-24HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
76299-321-852023-02-15These highlights do not include all the information needed to use STENDRA safely and effectively. See full prescribing information for STENDRA . STENDRA ® (avanafil) tablets, for oral use Initial U.S. Approval: 2012
76299-321-882023-02-15These highlights do not include all the information needed to use STENDRA safely and effectively. See full prescribing information for STENDRA . STENDRA ® (avanafil) tablets, for oral use Initial U.S. Approval: 2012
76299-321-962023-02-15These highlights do not include all the information needed to use STENDRA safely and effectively. See full prescribing information for STENDRA . STENDRA ® (avanafil) tablets, for oral use Initial U.S. Approval: 2012
76299-321-852023-01-30These highlights do not include all the information needed to use STENDRA safely and effectively. See full prescribing information for STENDRA . STENDRA ® (avanafil) tablets, for oral use Initial U.S. Approval: 2012
76299-321-882023-01-30These highlights do not include all the information needed to use STENDRA safely and effectively. See full prescribing information for STENDRA . STENDRA ® (avanafil) tablets, for oral use Initial U.S. Approval: 2012
76299-321-962023-01-30These highlights do not include all the information needed to use STENDRA safely and effectively. See full prescribing information for STENDRA . STENDRA ® (avanafil) tablets, for oral use Initial U.S. Approval: 2012
76299-321-852020-07-02These highlights do not include all the information needed to use STENDRA safely and effectively. See full prescribing information for STENDRA . STENDRA ® (avanafil) tablets, for oral use Initial U.S. Approval: 2012
76299-321-882020-07-02These highlights do not include all the information needed to use STENDRA safely and effectively. See full prescribing information for STENDRA . STENDRA ® (avanafil) tablets, for oral use Initial U.S. Approval: 2012
76299-321-962020-07-02These highlights do not include all the information needed to use STENDRA safely and effectively. See full prescribing information for STENDRA . STENDRA ® (avanafil) tablets, for oral use Initial U.S. Approval: 2012
76299-321-852020-01-31These highlights do not include all the information needed to use STENDRA safely and effectively. See full prescribing information for STENDRA . STENDRA ® (avanafil) tablets, for oral use Initial U.S. Approval: 2012
76299-321-882020-01-31These highlights do not include all the information needed to use STENDRA safely and effectively. See full prescribing information for STENDRA . STENDRA ® (avanafil) tablets, for oral use Initial U.S. Approval: 2012
76299-321-962020-01-31These highlights do not include all the information needed to use STENDRA safely and effectively. See full prescribing information for STENDRA . STENDRA ® (avanafil) tablets, for oral use Initial U.S. Approval: 2012

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
76299-321-85EA - Each76299-321afabd2ea-ffbc-4328-acef-1ea2a234c3ce12017-08-11

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 17 of 36 · 710 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Ultra StrengthANTACID TABLETSSAFEWAY4c6cdd81-5145-4a1f-888f-85cf5d856c392025-10-29WarningsExact identifier
unii: H0G9379FGK
Extra Strength SmoothANTACID TABLETSSAFEWAY8ed35c3b-9878-4889-90f7-a3973cf806e02025-10-29WarningsExact identifier
unii: H0G9379FGK
Publix Regular Strength Assorted FruitCALCIUM CARBONATEPUBLIX SUPER MARKETS, INCfd637431-7a08-4454-9cae-a68716d2d0fa2025-10-28WarningsExact identifier
unii: H0G9379FGK
Publix Regular Strength Peppermint FlavorCALCIUM CARBONATEPUBLIX SUPER MARKETS, INCc41b6cc2-c852-45fd-858c-c7bedc5dc8822025-10-28WarningsExact identifier
unii: H0G9379FGK
Publix Extra Strength Assorted BerryCALCIUM CARBONATEPUBLIX SUPER MARKETS, INCa270fc36-f2b2-4f56-81d4-cf165f6b5abe2025-10-28WarningsExact identifier
unii: H0G9379FGK
Extra Strength Sugar Free Orange Cream FlavorCALCIUM CARBONATEPUBLIX SUPER MARKETS, INC4dbdabc4-280d-4c9a-8c54-84afc615c8c72025-10-28WarningsExact identifier
unii: H0G9379FGK
Publix Extra Strength Tropical FruitCALCIUM CARBONATEPUBLIX SUPER MARKETS, INC28e8dd03-25cf-43db-8c4d-3aae99be9d532025-10-28WarningsExact identifier
unii: H0G9379FGK
Publix Ultra Strength Assorted FruitCALCIUM CARBONATEPUBLIX SUPER MARKETS, INC9e1c883f-016e-4c05-b27a-750d14c0f3e52025-10-28WarningsExact identifier
unii: H0G9379FGK
Ultra Strength AntacidCALCIUM CARBONATEWal-Mart Stores,Inc.,48827658-02f7-4599-a90a-1543b30b9de12025-10-27WarningsExact identifier
unii: H0G9379FGK
Regular Strength AntacidANTACIDWal-Mart Stores,Inc.,6e7cd170-b169-4fc0-bc90-f4421bbd9fcd2025-10-27WarningsExact identifier
unii: H0G9379FGK
equate Extra Strength AntacidCALCIUM CARBONATEWal-Mart Stores,Inc.,febe9d70-9a1f-43a9-8ad0-3134eefc69672025-10-27WarningsExact identifier
unii: H0G9379FGK
equate Extra Strength AntacidCALCIUM CARBONATEWal-Mart Stores,Inc.,d399f927-e80b-4162-a1f1-ef6159d6f7b12025-10-27WarningsExact identifier
unii: H0G9379FGK
equate Sugar Free Extra Strength Antacid Orange Cream FlavorANTACIDWal-Mart Stores,Inc.,53a22b37-66af-4735-b262-15e06ad7bf762025-10-27WarningsExact identifier
unii: H0G9379FGK
equate Extra Strength AntacidCALCIUM CARBONATEWal-Mart Stores,Inc.841ddf88-a016-4a3c-9508-5d5702883d8f2025-10-27WarningsExact identifier
unii: H0G9379FGK
Ultra Strength Antacid Assorted FruitCALCIUM CARBONATEWal-Mart Stores,Inc.,6900fabc-2299-48cf-bbda-c92649cfd0e12025-10-27WarningsExact identifier
unii: H0G9379FGK
equate Ultra Strength Antacid Peppermint FlavorANTACID TABLETSWal-Mart Stores,Inc.,6a18cd92-cc51-401b-9074-fbaa1afb42ac2025-10-27WarningsExact identifier
unii: H0G9379FGK
Extra Strength Smooth AntacidANTACID TABLETSWal-Mart Stores,Inc.,9acdfb08-043d-48a5-95f9-54bcba733c6e2025-10-27WarningsExact identifier
unii: H0G9379FGK
Extra Strength Smooth AntacidANTACID TABLETSWal-Mart Stores,Inc.,92372491-000d-4273-a668-b87722c1d3812025-10-27WarningsExact identifier
unii: H0G9379FGK
equate Extra Strength Smooth Antacid Assorted BerriesANTACID TABLETSWal-Mart Stores,Inc.,cc93e3b4-adbc-4a2c-b6fc-bf7456ef16562025-10-27WarningsExact identifier
unii: H0G9379FGK
Rugby Extra Strength Assorted BerriesANTACID TABLETSRugby Laboratoriesb0fcfd66-276e-4741-9aee-915b6364f25c2025-10-25WarningsExact identifier
unii: H0G9379FGK

Reported adverse events (FAERS/openFDA)#

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