NDC 68071-4909 Nitroglycerin Lingual
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What is NDC 68071-4909?
What are the uses for Nitroglycerin Lingual?
Which are Nitroglycerin Lingual UNII Codes?
The UNII codes for the active ingredients in this product are:
- NITROGLYCERIN (UNII: G59M7S0WS3)
- NITROGLYCERIN (UNII: G59M7S0WS3) (Active Moiety)
Which are Nitroglycerin Lingual Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- PEPPERMINT OIL (UNII: AV092KU4JH)
What is the NDC to RxNorm Crosswalk for Nitroglycerin Lingual?
- RxCUI: 705129 - nitroglycerin 400 MCG/ACTUAT Mucosal Spray
- RxCUI: 705129 - nitroglycerin 0.4 MG/ACTUAT Mucosal Spray
- RxCUI: 705129 - nitroglycerin 400 MCG/ACTUAT Oral Spray
- RxCUI: 705129 - nitroglycerin 400 MCG/ACTUAT Sublingual Spray
- RxCUI: 705129 - NTG 0.4 MG/ACTUAT Mucosal Spray
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Patient Education
Nitroglycerin Spray
Nitroglycerin spray is used to treat episodes of angina (chest pain) in people who have coronary artery disease (narrowing of the blood vessels that supply blood to the heart). The spray may also be used just before activities that may cause episodes of angina in order to prevent the angina from occurring. Nitroglycerin is in a class of medications called vasodilators. It works by relaxing the blood vessels so the heart does not need to work as hard and therefore does not need as much oxygen.
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".