NDC 68382-309 Nitroglycerin Transdermal System
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68382 - Zydus Pharmaceuticals Usa Inc.
- 68382-309 - Nitroglycerin Transdermal System
Product Packages
NDC Code 68382-309-30
Package Description: 30 POUCH in 1 CARTON / 1 PATCH in 1 POUCH (68382-309-01) / 14 h in 1 PATCH
Price per Unit: $0.54274 per EA
Product Details
What is NDC 68382-309?
What are the uses for Nitroglycerin Transdermal System?
Which are Nitroglycerin Transdermal System UNII Codes?
The UNII codes for the active ingredients in this product are:
- NITROGLYCERIN (UNII: G59M7S0WS3)
- NITROGLYCERIN (UNII: G59M7S0WS3) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Nitroglycerin Transdermal System?
- RxCUI: 486146 - nitroglycerin 0.6 MG/HR 24HR Transdermal System
- RxCUI: 486146 - 24 HR nitroglycerin 0.6 MG/HR Transdermal System
- RxCUI: 486146 - 24 HR NTG 0.6 MG/HR Transdermal System
- RxCUI: 486146 - 24 HR TNG 0.6 MG/HR Transdermal System
- RxCUI: 486146 - nitroglycerin 14 MG/Day 24 HR Transdermal Patch
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Patient Education
Nitroglycerin Transdermal Patch
Nitroglycerin transdermal patches are used to prevent episodes of angina (chest pain) in people who have coronary artery disease (narrowing of the blood vessels that supply blood to the heart). Nitroglycerin transdermal patches can only be used to prevent attacks of angina; they cannot be used to treat an attack of angina once it has begun. Nitroglycerin is in a class of medications called vasodilators. It works by relaxing the blood vessels so that 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".