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
Label	Manufacturer	Effective date	Type
Stendra - Mist Pharmaceuticals, LLC	Mist Pharmaceuticals, LLC	2021-05-24	HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
76299-321-85	2023-02-15	These 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
76299-321-88	2023-02-15	These 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
76299-321-96	2023-02-15	These 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
76299-321-85	2023-01-30	These 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
76299-321-88	2023-01-30	These 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
76299-321-96	2023-01-30	These 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
76299-321-85	2020-07-02	These 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
76299-321-88	2020-07-02	These 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
76299-321-96	2020-07-02	These 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
76299-321-85	2020-01-31	These 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
76299-321-88	2020-01-31	These 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
76299-321-96	2020-01-31	These 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 NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
76299-321-85	EA - Each	76299-321	afabd2ea-ffbc-4328-acef-1ea2a234c3ce	1	2017-08-11

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 35 of 36 · 710 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
GUNA LIVER PLUS	SODIUM PYRUVATE - SILYBUM MARIANUM SEED - CHELIDONIUM MAJUS - FUMARIC ACID - PORK LIVER - TARAXACUM OFFICINALE - LYCOPODIUM CLAVATUM SPORE - SODIUM SULFATE - PHOSPHORUS - BERBERIS VULGARIS ROOT BARK	Guna spa	ba44c46e-4509-2e4d-e053-2a95a90a9c95	2021-12-15	Warnings	Exact identifier unii: 88XHZ13131
GUNA OSTEO	ARNICA MONTANA ROOT - CALCIUM FLUORIDE - CALCIUM PHOSPHATE - EQUISETUM HYEMALE - FUMARIC ACID - SUS SCROFA UMBILICAL CORD - SUS SCROFA OVARY - SUS SCROFA PLACENTA - COMFREY ROOT - SUCCINIC ACID - SILICON DIOXIDE -	Guna spa	ba4462d6-9751-530f-e053-2995a90a1f16	2021-02-17	Warnings	Exact identifier unii: 88XHZ13131
GUNA LYMPHO DETOX	AESCULUS HIPPOCASTANUM - APIS MELLIFERA - CALENDULA OFFICINALIS FLOWER - HEXAKETOCYCLOHEXANE - EQUISETUM HYEMALE - FUMARIC ACID - GRAPHITE - HYDRASTIS CANADENSIS - HYDROCOTYLE ASIATICA - JUGLANS REGIA - LEVOTHYROXINE - MAGNESIUM PHOSPHATE - MALIC ACID - MYOSOTIS ARVENSIS - PHYTOLACCA AMERICANA ROOT - SARSAPARILLA - SODIUM DIETHYL OXALACETATE - SODIUM PYRUVATE - SUS SCROFA PLACENTA - TARAXACUM OFFICINALE -	Guna spa	aeb71e21-2fdb-6b84-e053-2995a90a4c01	2020-10-23	Warnings	Exact identifier unii: 88XHZ13131
GUNA-LIVER	CEANOTHUS AMERICANUS LEAF - CHELIDONIUM MAJUS - CHIONANTHUS VIRGINICUS BARK - CHOLINE HYDROXIDE - COBALAMIN - CULVER ROOT - FUMARIC ACID - INOSITOL - LYCOPODIUM CLAVATUM SPORE - NIACIN - PORK LIVER - POTASSIUM SULFATE - PYRIDOXINE HYDROCHLORIDE - RIBOFLAVIN - SILYBUM MARIANUM SEED - SODIUM DIETHYL OXALACETATE - SODIUM PYRUVATE - SODIUM SULFATE - SUS SCROFA GALL BLADDER - SUS SCROFA JEJUNUM - SUS SCROFA PANCREAS - SUS SCROFA SPLEEN - TARAXACUM OFFICINALE - THIAMINE HYDROCHLORIDE -	Guna spa	ab42235e-6080-492c-b5f2-fdbeb663a24d	2018-12-21	Warnings	Exact identifier unii: 88XHZ13131
GUNA-HYPERTENSION	ARNICA MONTANA - FUMARIC ACID - GOLD - LEAD - MELATONIN - MELILOTUS - OLEA EUROPAEA FLOWER - PORK KIDNEY - RAUWOLFIA SERPENTINA - SODIUM PYRUVATE - SPIGELIA - SUS SCROFA ADRENAL GLAND - SUS SCROFA DIENCEPHALON - UBIDECARENONE - VISCUM ALBUM FRUIT -	Guna spa	40c5b156-dc5c-41c2-88c3-a9bf28119d22	2018-12-21	Warnings	Exact identifier unii: 88XHZ13131
GUNA-DIZZY	.ALPHA.-KETOGLUTARIC ACID - AMBERGRIS - ANAMIRTA COCCULUS SEED - CONIUM MACULATUM FLOWERING TOP - EPINEPHRINE - FUMARIC ACID - MALIC ACID - MELATONIN - MINERAL OIL - PTERIDIUM AQUILINUM ROOT - PYRIDOXINE HYDROCHLORIDE - QUINHYDRONE - QUININE - SUS SCROFA ARTERY - SUS SCROFA CEREBELLUM - SUS SCROFA PLACENTA - THIAMINE HYDROCHLORIDE - TOBACCO LEAF -	Guna spa	c5f4a798-e628-4388-a98d-7449dd92f2d6	2018-12-21	Warnings	Exact identifier unii: 88XHZ13131
OMEOSPORT	.ALPHA.-KETOGLUTARIC ACID - ACONITIC ACID, CIS - ADENOSINE TRIPHOSPHATE - ALPHA LIPOIC ACID - ASCORBIC ACID - ASIAN GINSENG - BARIUM CATION - BEET - CEROUS OXALATE NONAHYDRATE - COENZYME A - CYSTEINE - FUMARIC ACID - LACTIC ACID, DL - MAGNESIUM CARBONATE - MALIC ACID - MANGANESE PHOSPHATE, DIBASIC - PORK - PYRIDOXINE HYDROCHLORIDE - RIBOFLAVIN - SODIUM DIETHYL OXALACETATE - SODIUM PYRUVATE - SUCCINIC ACID - SUS SCROFA ADRENAL GLAND - THIAMINE HYDROCHLORIDE - SUS SCROFA EMBRYO -	Guna spa	119a205d-0074-48ff-ac78-e2300db45227	2018-12-21	Warnings	Exact identifier unii: 88XHZ13131
Diathesis I	MANGANUM METALLICUM, GERMANIUM SESQUIOXIDE, FEL TAURI, HEPAR SUIS, GINKGO BILOBA, CYSTEINUM, MANGANESE GLUCONATE, ALPHA-KETOGLUTARICUM ACIDUM, ARSENICUM ALBUM, FUMARICUM ACIDUM, PHOSPHORUS, SODIUM OXALATE, SULPHUR	BioActive Nutritionals, Inc.	e8c3b763-7d54-48b1-8db8-a5b47ce7aeeb	2018-07-13	Warnings	Exact identifier unii: 88XHZ13131
up and up extra strength smooth dissolving antacid Assorted Fruit	ANTACID TABLETS	Target corporation	f2c0f9e5-61bd-4fb0-a29e-d358609c9270	2018-01-18	Warnings	Exact identifier unii: H0G9379FGK
Heartburn Plus Gas Relief Chewable Multi Symptom	CALCIUM CARBONATE ,MAGNESIUM HYDROXIDE,SIMETHICONE	WALGREEN CO.	2c02e195-9c17-4ddc-80c2-52e51ae9eba0	2018-01-01	Warnings	Exact identifier unii: H0G9379FGK
EQUALINE regular strength antacid	ANTACID	SUPERVALU INC	8091fc56-41b1-4f68-962a-534ecdb6f238	2017-12-27	Warnings	Exact identifier unii: H0G9379FGK
EQUALINE extra strength antacid	ANTACID	SUPERVALU INC	8630a040-92ce-47a3-b1b3-888a58a9d457	2017-12-27	Warnings	Exact identifier unii: H0G9379FGK
Diathesis II	GERMANIUM SESQUIOXIDE, CUPRUM METALLICUM, MANGANUM METALLICUM, INTESTINE (SUIS), LUNG (SUIS), CYSTEINUM, MANGANESE GLUCONATE, ALPHA-KETOGLUTARICUM ACIDUM, ARSENICUM ALBUM, CALCAREA CARBONICA, FUMARICUM ACIDUM, NATRUM OXALACETICUM, PHOSPHORUS	BioActive Nutritional, Inc.	240a5573-0603-4201-ab11-39b894b8794e	2017-12-27	Warnings	Exact identifier unii: 88XHZ13131
ANTACID	CALCIUM CARBONATE	Advance Pharmaceutical Inc.	0108b97f-02e9-4f86-9f33-cde4f919affd	2017-12-22	Warnings	Exact identifier unii: H0G9379FGK
Extra Strength Antacid	CALCIUM CARBONATE	PuraCap Pharmaceutical LLC	80509620-a3d1-49d5-b2e3-bff61ef4583d	2017-12-13	Warnings	Exact identifier unii: H0G9379FGK
Extra Strength Antacid	CALCIUM CARBONATE	CVS PHARMACY, INC.	80e10be2-879b-47ba-b34d-a3c25e838e05	2017-12-13	Warnings	Exact identifier unii: H0G9379FGK
Calcium Antacid	CALCIUM CARBONATE	Allegiant Health	51dd53e8-22ff-4967-9124-f15c3986e4dd	2017-11-17	Warnings	Exact identifier unii: H0G9379FGK
Calcium Antacid	CALCIUM CARBONATE	Allegiant Health	551d6135-2650-4c27-a20d-d56a9aba7b71	2017-11-08	Warnings	Exact identifier unii: H0G9379FGK
ANTACID	CALCIUM CARBONATE	Richmond Pharmaceuticals, Inc.	bc9467ac-4688-401b-af4b-a892c783921d	2017-10-30	Warnings	Exact identifier unii: H0G9379FGK
Ultra Strength Antacid Tropical fruit	CALCIUM ANTACID	CVS	bc15041e-cb3a-4ea0-9477-5b0849b45b51	2017-10-03	Warnings	Exact identifier unii: H0G9379FGK

Reported adverse events (FAERS/openFDA)#

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