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 18 of 36 · 710 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
RugbyANTACID TABLETSRugby Laboratories9cb56bc3-7075-4f81-bd10-7e602034b7d82025-10-25WarningsExact identifier
unii: H0G9379FGK
Rugby Cal-Gest Antacid Assorted FlavorsANTACID TABLETSRugby Laboratories, Inc.a43184c4-d225-4539-b651-4d96535f208f2025-10-25WarningsExact identifier
unii: H0G9379FGK
MannitolMANNITOLICU Medical Inc.ba7bf864-8a4d-4262-8fd1-00174fa2f9d12025-10-24Warnings, Adverse reactionsExact identifier
unii: 3OWL53L36A
Exchange Select Antacid Soft Chews Cherry FlavorCALCIUM CARBONATEArmy & Air Force Exchange Service41ad5581-5b8a-1c8b-e063-6294a90a2ba62025-10-21WarningsExact identifier
unii: H0G9379FGK
acid reducer completeFAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDESafeway4f0a178c-d0ed-4bbc-a8ce-fda3789d25f02025-10-14WarningsExact identifier
unii: H0G9379FGK
CardinalExtra Strength Antacid Wintergreen flavorCALCIUM CARBONATECARDINAL HEALTH4e40989f-c710-442a-bb8d-02e813ddf04d2025-10-14WarningsExact identifier
unii: H0G9379FGK
Regular Strength Antacid Assorted FruitCALCIUM CARBONATECARDINAL HEALTHdef9eaef-308f-49f2-898b-469c2c395d272025-10-14WarningsExact identifier
unii: H0G9379FGK
Leader Extra Strength Sugar Free AntacidANTACIDCardinal Healthd7a6f1b8-bdf7-45bb-bab0-b22f45e784402025-10-14WarningsExact identifier
unii: H0G9379FGK
Cardinal Extra Strength Smooth Antacid Assorted FruitsCALCIUM CARBONATECARDINAL HEALTH84bf7fea-a071-4583-9453-1aea4d198ca62025-10-14WarningsExact identifier
unii: H0G9379FGK
ANTACID Extra StrengthCALCIUM CARBONATECardinal Health 110, LLC.3ce9b97b-1680-4299-9a2c-132318adbc0c2025-10-14WarningsExact identifier
unii: H0G9379FGK
ANTACID Extra StrengthCALCIUM CARBONATECARDINAL HEALTH 110, LLC.7c1b2ee6-b691-4c12-bed5-f0a360ad46bb2025-10-14WarningsExact identifier
unii: H0G9379FGK
ANTACID Ultra StrengthCALCIUM CARBONATECARDINAL HEALTH 110, LLC.d267ca31-09bd-46d3-be08-a259642f1b7f2025-10-14WarningsExact identifier
unii: H0G9379FGK
Kidnex IVGINKGO BILOBA, ALPHA-KETOGLUTARICUM ACIDUM, CITRICUM ACIDUM, FUMARICUM ACIDUM, MALICUM ACIDUM, PYRUVIC ACID, SUCCINICUM ACIDUM, ARGENTUM METALLICUM, AURUM METALLICUM, CUPRUM METALLICUM, GERMANIUM SESQUIOXIDE, MERCURIUS VIVUS, NUX VOMICA, KIDNEY (SUIS), LYMPH NODE (SUIS), NAPHTHOCHINONUM, NATRUM OXALACETICUM, PHOSPHORUS, URINARY BLADDER (SUIS), ACONITICUM ACIDUM, CIS-Energique, Inc.121eb51a-befe-47ea-85c6-d77e8c7e58642025-10-06WarningsExact identifier
unii: 88XHZ13131
Calcium Carbonate Antacid Assorted BerriesCALCIUM CARBONATEXiamen Kang Zhongyuan Biotechnology Co., Ltd.3f640ccd-4b8d-fc24-e063-6294a90a6e582025-09-22WarningsExact identifier
unii: H0G9379FGK
MGC Health Antacid Soft Chews Cherry FlavorCALCIUM CARBONATEMedical Group Care LLC3ea07f5f-59b2-eb0a-e063-6394a90a66b92025-09-12WarningsExact identifier
unii: H0G9379FGK
Up and Up Dual Action Acid Reducer and AntacidFAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDETarget Corporation2f020677-77a0-4e13-9397-e9deeda632932025-09-10WarningsExact identifier
unii: H0G9379FGK
McKesson Antacid Calcium CarbonateCALCIUM CARBONATEMcKesson Medical-Surgicalbdac6778-384c-50bb-e053-2995a90a0e172025-09-08WarningsExact identifier
unii: H0G9379FGK
Thompson AntacidCALCIUM CARBONATEThompsond9524a64-6f35-24a8-e053-2995a90a6ca32025-09-08WarningsExact identifier
unii: H0G9379FGK
Medique AlcalakCALCIUM CARBONATEUnifirst First Aid Corporation60703e3d-52b1-49c4-b4e2-59d96fa09a782025-09-08WarningsExact identifier
unii: H0G9379FGK
Belmora MELOX AGRURACALCIUM CARBONATEBelmora, LLC875f38f8-4e6f-7517-e053-2995a90a21812025-09-08WarningsExact identifier
unii: H0G9379FGK

Reported adverse events (FAERS/openFDA)#

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