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 24 of 36 · 710 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Extra Strength Smooth Peppermint AntacidCALCIUM CARBONATEDiscount Drug Mart, Inc2df8fe2b-cc9a-f026-e063-6394a90aa0ad2025-02-20WarningsExact identifier
unii: H0G9379FGK
Extra Strength AntacidCALCIUM CARBONATEHarris Teeter, LLC2cb4ce4e-e18c-c96d-e063-6394a90a18ca2025-02-20WarningsExact identifier
unii: H0G9379FGK
Extra Strength Smooth AntacidCALCIUM CARBONATEHarris Teeter, LLC2cb60b7e-711a-8052-e063-6394a90acf1d2025-02-20WarningsExact identifier
unii: H0G9379FGK
Extra Strength AntacidCALCIUM CARBONATEDiscount Drug Mart, Inc2df9e47a-8741-6958-e063-6394a90a6c602025-02-20WarningsExact identifier
unii: H0G9379FGK
Regular Strength Antacid PeppermintCALCIUM CARBONATEDiscount Drug Mart, Inc2e09b8d1-25b4-0e57-e063-6394a90a31e22025-02-20WarningsExact identifier
unii: H0G9379FGK
Bestmade Natural Products BM159ALETRIS FARINOSA, ASHOKA JANO, FLUORIC ACID, FUMARIC ACID, HYDRASTIS, HYDROCOTYLE ASIATICA, KALI BICH, KREASOTEBestmade Natural Products2e6c7481-b1cb-e3a6-e063-6294a90af0872025-02-18WarningsExact identifier
unii: 88XHZ13131
Tums Chewy Bites Orange and Cream ESCALCIUM CARBONATEHaleon US Holdings LLC036ef1ed-32ef-46b8-8817-b3f63a0142802025-02-14WarningsExact identifier
unii: H0G9379FGK
Tums NaturalsCALCIUM CARBONATEHaleon US Holdings LLCd8da54b8-6456-4e7d-acd2-a55e2249bd012025-02-13WarningsExact identifier
unii: H0G9379FGK
Ultra Strength Antacid Assorted FruitCALCIUM CARBONATEHarris Teeter, LLC2cb4c58f-ee88-b60e-e063-6294a90a1e6c2025-02-12WarningsExact identifier
unii: H0G9379FGK
Regular Strength Antacid PeppermintCALCIUM CARBONATEHarris Teeter, LLC2cb54a40-98ce-2660-e063-6294a90a3ed02025-02-11WarningsExact identifier
unii: H0G9379FGK
Extra Strength Antacid Tropical FruitCALCIUM CARBONATEHarris Teeter, LLC2c65f7f5-195c-ed33-e063-6294a90a30702025-02-11WarningsExact identifier
unii: H0G9379FGK
Regular Strength AntacidCALCIUM CARBONATEHarris Teeter, LLC2cb50083-b05f-8aca-e063-6394a90a6d6f2025-02-11WarningsExact identifier
unii: H0G9379FGK
Extra Strength AntacidCALCIUM CARBONATEHarris Teeter, LLC2c544c08-8cdb-edf2-e063-6394a90a024c2025-02-11WarningsExact identifier
unii: H0G9379FGK
Extra Strength Antacid Tropical FruitCALCIUM CARBONATEUNITED NATURAL FOODS, INC. DBA UNFI1b6a28a2-f848-d185-e063-6294a90ab3382025-02-07WarningsExact identifier
unii: H0G9379FGK
Genexa Antacid Maximum StrengthCALCIUM CARBONATEGenexa Inc.e4b8f068-ad52-10c8-e053-2a95a90a871f2025-02-07WarningsExact identifier
unii: H0G9379FGK
Regular Strength Peppermint AntacidCALCIUM CARBONATEDeMoulas Market Basket89bdb1c0-df39-4c37-bb0d-0bfd0bff85fb2025-02-07WarningsExact identifier
unii: H0G9379FGK
Ultra Strength AntacidCALCIUM CARBONATEUNITED NATURAL FOODS, INC. DBA UNFI1cbea7c2-fdc0-5a6b-e063-6294a90a9cfa2025-02-07WarningsExact identifier
unii: H0G9379FGK
Regular Strength AntacidCALCIUM CARBONATEDeMoulas Market Basketbe167e45-3db8-4739-91ac-e83d552236172025-02-07WarningsExact identifier
unii: H0G9379FGK
Extra Strength Smooth AntacidCALCIUM CARBONATEUNITED NATURAL FOODS, INC. DBA UNFI1b6a4808-4d0b-783c-e063-6394a90af0c32025-02-07WarningsExact identifier
unii: H0G9379FGK
Ultra Strength Antacid Assorted BerriesCALCIUM CARBONATEGuardian Drug Company7f0ca229-7452-4f18-bd2f-bf2dfc3482f82025-02-06WarningsExact identifier
unii: H0G9379FGK

Reported adverse events (FAERS/openFDA)#

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