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 12 of 36 · 710 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Good Sense Antacid Soft ChewCALCIUM CARBONATEGeiss, Destin Dunnc7420218-b20e-0f0d-e053-2995a90a23862025-12-12WarningsExact identifier
unii: H0G9379FGK
cherry antacid soft chewCALCIUM CARBONATEAmerican Sales49261864-e596-20e5-e054-00144ff8d46c2025-12-07WarningsExact identifier
unii: H0G9379FGK
Assorted Fruit Antacid Flavor ChewsCALCIUM CARBONATECVS Pharmacy3c679059-2532-485a-e054-00144ff88e882025-12-07WarningsExact identifier
unii: H0G9379FGK
Antacid Fruit ChewsCALCIUM CARBONATECVS Pharmacy4a527608-b4d4-57c0-e054-00144ff88e882025-12-07WarningsExact identifier
unii: H0G9379FGK
Heartburn and gas fruit chewsCALCIUM CARBONATECVS Pharmacy4a656a9f-8f34-69b7-e054-00144ff8d46c2025-12-07WarningsExact identifier
unii: H0G9379FGK
Orange Antacid Soft ChewCALCIUM CARBONATECVS Pharmacy4a67f0d0-788b-433b-e054-00144ff88e882025-12-07WarningsExact identifier
unii: H0G9379FGK
Cherry Antacid Soft ChewsCALCIUM CARBONATECVS Pharmacy61e4e83c-ee98-579d-e053-2991aa0ab0992025-12-07WarningsExact identifier
unii: H0G9379FGK
CVS Mixed Berry Antacid HBG 54ctCALCIUM CARBONATECVS Pharmacye9204edb-e4d9-3975-e053-2995a90ac6a92025-12-07WarningsExact identifier
unii: H0G9379FGK
CVS Mixed Berry Antacid HBG 28ctCALCIUM CARBONATECVS Pharmacye9481d36-3b28-5caf-e053-2a95a90a31212025-12-07WarningsExact identifier
unii: H0G9379FGK
CVS Wild Berry Antacid ChewsCALCIUM CARBONATECVS Pharmacyf6f45d9c-f9fc-225b-e053-6394a90a30e12025-12-07WarningsExact identifier
unii: H0G9379FGK
CVS Wild Berry Antacid ChewsCALCIUM CARBONATECVS Pharmacyf6f5dc9a-b573-70c1-e053-6394a90acdb02025-12-07WarningsExact identifier
unii: H0G9379FGK
Basic Care Antacid Fruit ChewsCALCIUM CARBONATEAmazon.comc8d2b8aa-fce4-f973-e053-2995a90a6edd2025-12-05WarningsExact identifier
unii: H0G9379FGK
Basic Care Berry Antacid HBGCALCIUM CARBONATEAmazon.comc8d4050e-75fd-2445-e053-2995a90a7b0d2025-12-05WarningsExact identifier
unii: H0G9379FGK
CVS Health Maximum StrengthANTACID AND ANTIGASCVS Pharmacy,Inc.0a13ac81-0c63-48c1-bbb0-f6e67f97b8962025-12-04WarningsExact identifier
unii: H0G9379FGK
QUALITY CHOICE Regular StrengthANTACID TABLETS (CALCIUM CARBONATE)QUALITY CHOICE (Chain drug Marketing Assoiciation)fce6c50d-908f-44a6-ba63-ece813f3711b2025-12-04WarningsExact identifier
unii: H0G9379FGK
QUALITY CHOICE Regular StrengthANTACID TABLETS (CALCIUM CARBONATE)QUALITY CHOICE (Chain drug Marketing Assoiciation)667ffb59-9bff-45a7-89f0-ccfa0d8419092025-12-04WarningsExact identifier
unii: H0G9379FGK
QUALITY CHOICECALCIUM CARBONATEQUALITY CHOICE (Chain drug Marketing Assoiciation)9ff282fd-7623-4c9e-8faa-c51e33a7616e2025-12-04WarningsExact identifier
unii: H0G9379FGK
QUALITY CHOICE Extra StrengthANTACID TABLETS (CALCIUM CARBONATE)QUALITY CHOICE (Chain drug Marketing Assoiciation)7c948dc6-e569-46d2-8edd-59da48857e0e2025-12-04WarningsExact identifier
unii: H0G9379FGK
QUALITY CHOICE Ultra StrengthANTACID TABLETS (CALCIUM CARBONATE)QUALITY CHOICE (Chain drug Marketing Assoiciation)b074a885-5d10-46e4-8de9-dd9460968dad2025-12-04WarningsExact identifier
unii: H0G9379FGK
Quality Choice Extra StrengthANTACID TABLETS (CALCIUM CARBONATE)QUALITY CHOICE (Chain drug Marketing Assoiciation)2bb8ccb6-6275-4ace-8096-ee545501df392025-12-04WarningsExact identifier
unii: H0G9379FGK

Reported adverse events (FAERS/openFDA)#

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