NDC 21695-635 Nitroglycerin Slocaps
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-635 - Nitroglycerin Slocaps
Product Characteristics
Product Packages
NDC Code 21695-635-60
Package Description: 60 CAPSULE in 1 BOTTLE
Product Details
What is NDC 21695-635?
What are the uses for Nitroglycerin Slocaps?
Which are Nitroglycerin Slocaps UNII Codes?
The UNII codes for the active ingredients in this product are:
- NITROGLYCERIN (UNII: G59M7S0WS3)
- NITROGLYCERIN (UNII: G59M7S0WS3) (Active Moiety)
Which are Nitroglycerin Slocaps 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:
- GELATIN (UNII: 2G86QN327L)
- LACTOSE (UNII: J2B2A4N98G)
- STARCH, CORN (UNII: O8232NY3SJ)
- SUCROSE (UNII: C151H8M554)
- TALC (UNII: 7SEV7J4R1U)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
What is the NDC to RxNorm Crosswalk for Nitroglycerin Slocaps?
- RxCUI: 312013 - nitroglycerin 2.5 MG Extended Release Oral Capsule
- RxCUI: 312013 - NTG 2.5 MG Extended Release Oral Capsule
- RxCUI: 312013 - TNG 2.5 MG Extended Release Oral Capsule
- RxCUI: 312018 - nitroglycerin 6.5 MG Extended Release Oral Capsule
- RxCUI: 312018 - NTG 6.5 MG Extended Release Oral Capsule
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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".