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 11 of 36 · 710 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Target Berry Lime HBG ChewsCALCIUM CARBONATETarget11fba65d-8a81-1227-e063-6294a90a11bd2025-12-20WarningsExact identifier
unii: H0G9379FGK
Target Gas Relief Chews Mixed Berry and StrawberrySIMETHICONETarget11fd2ccd-3a2b-c141-e063-6394a90ab34f2025-12-20WarningsExact identifier
unii: H0G9379FGK
TopCare Cherry Antacid Soft ChewsCALCIUM CARBONATETopCodd93d53d-545a-b47c-e053-2a95a90a2a052025-12-20WarningsExact identifier
unii: H0G9379FGK
Ultra Strength Antacid Tropical Fruit FlavorCALCIUM CARBONATE7-ELEVEN2f3c61ef-06a3-8a96-e063-6294a90ab8d22025-12-19WarningsExact identifier
unii: H0G9379FGK
Ultra Strength Antacid Tropical Fruit FlavorCALCIUM CARBONATEXiamen Kang Zhongyuan Biotechnology Co., Ltd.2f3c3c65-4177-6304-e063-6294a90a51fa2025-12-19WarningsExact identifier
unii: H0G9379FGK
Cherry Antacid Relief ChewCALCIUM CARBONATERite Aid6417a5d4-cfc9-b701-e053-2a91aa0a55cd2025-12-19WarningsExact identifier
unii: H0G9379FGK
Rite Aid Wild Berry Antacid ChewsCALCIUM CARBONATERite Aiddeac0759-86b9-6214-e053-2a95a90aa4c42025-12-19WarningsExact identifier
unii: H0G9379FGK
Cherry Antacid Soft ChewsCALCIUM CARBONATEMeijer Distribution Inc.3ce1b794-cdd1-38ee-e054-00144ff8d46c2025-12-18WarningsExact identifier
unii: H0G9379FGK
Meijer Wild Berry Antacid ChewsCALCIUM CARBONATEMeijerd6961473-262d-2e87-e053-2995a90ae23a2025-12-18WarningsExact identifier
unii: H0G9379FGK
Meijer Wild Berry Antacid ChewsCALCIUM CARBONATEMeijerd6a6315f-19ca-e760-e053-2a95a90a83112025-12-18WarningsExact identifier
unii: H0G9379FGK
Meijer Berry Lime Antacid HBG ChewsCALCIUM CARBONATEMeijer16efa685-5b74-2661-e063-6394a90ac5062025-12-18WarningsExact identifier
unii: H0G9379FGK
Meijer Max Gas 30ctSIMETHICONEMeijer23f95dcf-3d4c-a119-e063-6394a90a51552025-12-18WarningsExact identifier
unii: H0G9379FGK
AvanafilAVANAFILCamber Pharmaceuticals, Inc.1d04e17d-7399-430a-a8bb-fa1912b155e92025-12-17Warnings, Adverse reactionsExact identifier
unii: DR5S136IVO
Antacid Regular strengthANTACID TABLETSWALGREEN CO.9090e2c0-4837-44ea-b6c4-f46532eadee12025-12-17WarningsExact identifier
unii: H0G9379FGK
Kroger Cherry Antacid Soft ChewCALCIUM CARBONATEKroger142d7c79-f87f-03fd-e063-6394a90adb0b2025-12-17WarningsExact identifier
unii: H0G9379FGK
CVS Orange Cream Antacid ChewsCALCIUM CARBONATECVS Pharmacy45f6b593-a09c-ce0b-e063-6394a90ae3072025-12-14WarningsExact identifier
unii: H0G9379FGK
Cherry Antacid Soft ChewCALCIUM CARBONATEHEB3b4e6ac5-4d9b-3e84-e054-00144ff88e882025-12-13WarningsExact identifier
unii: H0G9379FGK
HEB Wild Berry Antacid ChewsCALCIUM CARBONATEHEBd826abde-5090-1ace-e053-2995a90a8b4d2025-12-13WarningsExact identifier
unii: H0G9379FGK
HEB Wild Berry Antacid Chews 60ctCALCIUM CARBONATEHEBd827a6d6-3e01-6d73-e053-2995a90a791b2025-12-13WarningsExact identifier
unii: H0G9379FGK
Family Wellness Antacid Relief ChewsCALCIUM CARBONATEFamily Dollarf926c9a4-9c61-b7d5-e053-6294a90afff52025-12-12WarningsExact identifier
unii: H0G9379FGK

Reported adverse events (FAERS/openFDA)#

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