NDC 68151-1480 Diltiazem Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-1480 - Diltiazem Hydrochloride
Product Characteristics
Product Details
What is NDC 68151-1480?
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:
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- ETHYL ACRYLATE (UNII: 71E6178C9T)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GELATIN (UNII: 2G86QN327L)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POVIDONES (UNII: FZ989GH94E)
- SUCROSE STEARATE (UNII: 274KW0O50M)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
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".