NDC 21695-403 Diltiazem Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-403 - Diltiazem Hydrochloride
Product Characteristics
Product Packages
NDC Code 21695-403-30
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 21695-403?
What are the uses for Diltiazem Hydrochloride?
Which are Diltiazem Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- DILTIAZEM HYDROCHLORIDE (UNII: OLH94387TE)
- DILTIAZEM (UNII: EE92BBP03H) (Active Moiety)
Which are Diltiazem Hydrochloride 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:
- AMMONIO METHACRYLATE COPOLYMER TYPE A (UNII: 8GQS4E66YY)
- AMMONIO METHACRYLATE COPOLYMER TYPE B (UNII: 161H3B14U2)
- AMMONIA (UNII: 5138Q19F1X)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- GELATIN (UNII: 2G86QN327L)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- SHELLAC (UNII: 46N107B71O)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SUCROSE (UNII: C151H8M554)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
What is the NDC to RxNorm Crosswalk for Diltiazem Hydrochloride?
- RxCUI: 830837 - dilTIAZem HCl 240 MG 24HR Extended Release Oral Capsule
- RxCUI: 830837 - 24 HR diltiazem hydrochloride 240 MG Extended Release Oral Capsule
- RxCUI: 830837 - diltiazem HCl 240 MG 24 HR Extended Release Oral Capsule
- RxCUI: 830845 - dilTIAZem HCl 180 MG 24HR Extended Release Oral Capsule
- RxCUI: 830845 - 24 HR diltiazem hydrochloride 180 MG Extended Release Oral Capsule
* Please review the disclaimer below.
[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".