NDC 68258-6024 Diltiazem Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68258 - Dispensing Solutions, Inc.
- 68258-6024 - Diltiazem Hydrochloride
Product Characteristics
Product Packages
NDC Code 68258-6024-9
Package Description: 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 68258-6024?
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:
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:2) (UNII: 5KY68S2577)
- AMMONIA (UNII: 5138Q19F1X)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- GELATIN (UNII: 2G86QN327L)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SUCROSE (UNII: C151H8M554)
- STARCH, CORN (UNII: O8232NY3SJ)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
What is the NDC to RxNorm Crosswalk for Diltiazem Hydrochloride?
- RxCUI: 830861 - dilTIAZem HCl 120 MG 24HR Extended Release Oral Capsule
- RxCUI: 830861 - 24 HR diltiazem hydrochloride 120 MG Extended Release Oral Capsule
- RxCUI: 830861 - diltiazem HCl 120 MG 24 HR 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".