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 10 of 36 · 710 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
QC Ultra Strength Antacid Soft Chews, CherryQC ANTACID SOFT CHEWS, CHERRYXiamen Kang Zhongyuan Biotechnology Co., Ltd.26a97517-d3e7-d896-e063-6394a90acc952025-12-29WarningsExact identifier
unii: H0G9379FGK
Tums Chewy BitesCALCIUM CARBONATESelect Consumer Group3caa037e-3424-f9ce-e063-6294a90ac1e82025-12-27WarningsExact identifier
unii: H0G9379FGK
AntacidANTACIDXiamen Kang Zhongyuan Biotechnology Co., Ltd.17adb983-bb28-bf8b-e063-6394a90a7daa2025-12-26WarningsExact identifier
unii: H0G9379FGK
Assorted Fruit Antacid Flavor ChewsCALCIUM CARBONATEWalmart77cbc5e4-518e-7d86-e053-2991aa0a1efa2025-12-23WarningsExact identifier
unii: H0G9379FGK
Mixed Berry Antacid and Anti-Gas ChewsCALCIUM CARBONATEWalmart Stores41e63d39-bfcb-07a8-e054-00144ff88e882025-12-23WarningsExact identifier
unii: H0G9379FGK
Equate Wild Berry Antacid ChewsCALCIUM CARBONATEWalmart0994d92e-c1da-e36e-e063-6294a90aacdc2025-12-23WarningsExact identifier
unii: H0G9379FGK
ANTACID AND ANTIGASCALCIUM CARBONATE, MAGNESIUM HYDROXIDE, SIMETHICONEMeijer, Inc.419a7333-9743-8e31-e063-6394a90a49742025-12-23WarningsExact identifier
unii: H0G9379FGK
QC Ultra Strength Antacid Soft Chews, CherryQC ANTACID SOFT CHEWS, CHERRYChain Drug Marketing Association, Inc.266b777a-939e-c697-e063-6394a90a90a92025-12-22WarningsExact identifier
unii: H0G9379FGK
Caring Mill AntacidCARING MILL ANTACID CHERRY FLAVOR SOFT CHEWSFSA STORE INC.240dc06b-5c66-5e1f-e063-6394a90a42a22025-12-22WarningsExact identifier
unii: H0G9379FGK
Antacid Soft ChewCALCIUM CARBONATEWalgreen Co.479284ad-ec02-4b74-e054-00144ff8d46c2025-12-21WarningsExact identifier
unii: H0G9379FGK
Antacid Flavor ChewCALCIUM CARBONATEWalgreen Co.47dfbe23-f407-6588-e054-00144ff8d46c2025-12-21WarningsExact identifier
unii: H0G9379FGK
Antacid Flavor ChewsCALCIUM CARBONATEWalgreen Co.47e0830f-31e7-5ff0-e054-00144ff88e882025-12-21WarningsExact identifier
unii: H0G9379FGK
Walgreens Wild Berry Antacid ChewsCALCIUM CARBONATEWalgreens Companyeb523ea1-0919-0caa-e053-2a95a90a86ea2025-12-21WarningsExact identifier
unii: H0G9379FGK
Walgreens Wild Berry Antacid ChewsCALCIUM CARBONATEWalgreens09cf38c2-0b45-eca1-e063-6294a90a72d82025-12-21WarningsExact identifier
unii: H0G9379FGK
Walgreens Cherry Berry Lime Antacid HBG 54ctCALCIUM CARBONATEWalgreens21da4a30-403d-ec9c-e063-6394a90aa36b2025-12-21WarningsExact identifier
unii: H0G9379FGK
Cherry Antacid Soft ChewsCALCIUM CARBONATEWalmart Stores Inc.40f9338f-41ad-19a8-e054-00144ff8d46c2025-12-21WarningsExact identifier
unii: H0G9379FGK
Assorted Fruit Antacid ChewsCALCIUM CARBONATETarget Corporation40cd0ff8-c745-3b99-e054-00144ff88e882025-12-20WarningsExact identifier
unii: H0G9379FGK
Target Antacid Fruit ChewsCALCIUM CARBONATETarget964c07b7-4560-537c-e053-2995a90a2f4e2025-12-20WarningsExact identifier
unii: H0G9379FGK
Target Antacid - Anti-Gas Relief ChewsCALCIUM CARBONATETarget964e357c-a8ab-09fa-e053-2a95a90a37c62025-12-20WarningsExact identifier
unii: H0G9379FGK
Target Wild Berry Antacid Chews 60ctCALCIUM CARBONATETargetd8288751-f316-1dc0-e053-2995a90a139f2025-12-20WarningsExact identifier
unii: H0G9379FGK

Reported adverse events (FAERS/openFDA)#

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