NDC 54868-3300 Verapamil Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
15 MM
M;312
2
Code Structure Chart
Product Details
What is NDC 54868-3300?
What are the uses for Verapamil Hydrochloride?
Which are Verapamil Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- VERAPAMIL HYDROCHLORIDE (UNII: V3888OEY5R)
- VERAPAMIL (UNII: CJ0O37KU29) (Active Moiety)
Which are Verapamil 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:
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- POVIDONE (UNII: FZ989GH94E)
- SODIUM ALGINATE (UNII: C269C4G2ZQ)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Verapamil Hydrochloride?
- RxCUI: 897640 - verapamil HCl 180 MG Extended Release Oral Tablet
- RxCUI: 897640 - verapamil hydrochloride 180 MG Extended Release Oral Tablet
- RxCUI: 897649 - verapamil HCl 240 MG Extended Release Oral Tablet
- RxCUI: 897649 - verapamil hydrochloride 240 MG Extended Release Oral Tablet
- RxCUI: 897659 - verapamil HCl 120 MG Extended Release Oral Tablet
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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".