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 22 of 36 · 710 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Calcium Carbonate 750 mgCALCIUM CARBONATE 750 MG - ASSORTED BERRIESCVS Pharmacy.Inc.23a76a4f-8c41-b9d0-e063-6394a90a19c52025-04-09WarningsExact identifier
unii: H0G9379FGK
Bio Co Enzyme PhaseACONITICUM ACIDUM, CIS-, ADENOSINUM TRIPHOSPHORICUM DINATRUM, ADRENALINUM, , ALPHA-KETOGLUTARICUM ACIDUM, ALPHA-LIPOICUM ACIDUM, ASCORBICUM ACIDUM, BARIUM OXALSUCCINICUM, BETA VULGARIS, CERIUM OXALICUM, CITRICUM ACIDUM, CYSTEINUM, FUMARICUM ACIDUM, HEPAR SULPHURIS CALCAREUM, MAGNESIUM OROTICUM DIHYDRICUM, MALICUM ACIDUM, MANGANUM PHOSPHORICUM, NADIDUM, NATRUM OXALACETICUM, NATRUM PYRUVICUM, NICOTINAMIDUM, PANTOTHENIC ACID, PROTEUS (MORGANI), PULSATILLA (PRATENSIS), PYRIDOXINUM HYDROCHLORICUM, RIBOFLAVINUM,Deseret Biologicals, Inc.6edee6eb-0ec9-4d2a-9dc9-dc2a6503a6db2025-04-08WarningsExact identifier
unii: 88XHZ13131
BERKLEY JENSEN ULTRA STRENGTHANTACID CALCIUM CARBONATEBJWCc7eedcbf-3b07-4cd3-937b-c56d7cc5bc572025-04-08WarningsExact identifier
unii: H0G9379FGK
Extra Strength Antacid Smooth Dissolving - Assorted FruitCALCIUM CARBONATETARGET CORPORATION28fc38a7-f7a0-a6a5-e063-6294a90af94c2025-04-05WarningsExact identifier
unii: H0G9379FGK
Extra Strength Antacid Smooth dissolving - Berry Fusion FlavorsCALCIUM CARBONATETARGET CORPORATION28fce33f-c561-1512-e063-6294a90a111c2025-04-05WarningsExact identifier
unii: H0G9379FGK
Ultra Strength Antacid Assorted BerriesCALCIUM CARBONATERite Aid840a617d-d006-4a9b-b98a-8a5ed9af0f402025-03-31WarningsExact identifier
unii: H0G9379FGK
Ultra Strength Antacid PeppermintCALCIUM CARBONATERite Aid3cb46f74-7a62-4b27-beac-a3c055a282152025-03-31WarningsExact identifier
unii: H0G9379FGK
Calcium Carbonate 1000 mgCALCIUM CARBONATE 1000 MG - TROPICAL FRUITCVS HEALTH CORP24ceba32-eb32-902f-e063-6394a90a9fd52025-03-28WarningsExact identifier
unii: H0G9379FGK
Extra Strength Antacid Assorted BerriesCALCIUM CARBONATERite Aidb1af099d-4095-4bd7-a23c-ad85e92513d82025-03-28WarningsExact identifier
unii: H0G9379FGK
Extra Strength Antacid Orange Cream Sugar FreeCALCIUM CARBONATERite Aid089a1cd5-954e-4c3f-ab4b-cac693a1d44a2025-03-28WarningsExact identifier
unii: H0G9379FGK
Extra Strength Antacid Assorted FruitCALCIUM CARBONATERite Aide94557a0-528a-413d-846b-9568bbb7c35f2025-03-28WarningsExact identifier
unii: H0G9379FGK
Extra Strength Antacid Tropical FruitCALCIUM CARBONATERite Aid0c4d1c0e-09bb-49f6-97da-2b13ef5788e92025-03-28WarningsExact identifier
unii: H0G9379FGK
Extra Strength Smooth Antacid Assorted FruitCALCIUM CARBONATERite Aid470e57e6-eccb-4146-9a9e-ecaa0f013db02025-03-28WarningsExact identifier
unii: H0G9379FGK
Extra Strength Smooth Antacid Assorted BerriesCALCIUM CARBONATERite Aid7576ba40-2fa5-4ec7-8dc1-77a7b735a5162025-03-28WarningsExact identifier
unii: H0G9379FGK
Signature Care Acid Reducer CompleteFAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDESafeway249b19fd-d5b3-4c93-92bb-f277797015b42025-03-27WarningsExact identifier
unii: H0G9379FGK
TopCare Max Gas Antacid plus Anti-Gas ChewsSIMETHICONETopCo309e8215-84b0-dd84-e063-6394a90ac4422025-03-18WarningsExact identifier
unii: H0G9379FGK
TopCare Cherry Berry Lime Antacid HBGCALCIUM CARBONATETopCo30a01bf6-28c8-87ae-e063-6394a90a6fb52025-03-18WarningsExact identifier
unii: H0G9379FGK
Ultra strength AntacidCALCIUM CARBONATECVS HEALTH CORP2480eace-06a6-86a2-e063-6394a90a3c0c2025-03-15WarningsExact identifier
unii: H0G9379FGK
Extra Strength Assorted Fruit AntacidCALCIUM CARBONATEHarris Teeter, LLC2c51d1e6-fee2-c092-e063-6294a90acbe92025-03-14WarningsExact identifier
unii: H0G9379FGK
Supreme AntacidCALCIUM CARBONATE, MAGNESIUM HYDROXIDEH E B18a7dfd9-d927-7625-e063-6394a90a270f2025-03-14WarningsExact identifier
unii: H0G9379FGK

Reported adverse events (FAERS/openFDA)#

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