NDC 54868-0120 Verapamil Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-0120 - Verapamil Hydrochloride
Product Characteristics
Product Packages
NDC Code 54868-0120-2
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
NDC Code 54868-0120-3
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 54868-0120?
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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- STARCH, CORN (UNII: O8232NY3SJ)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLACRILIN POTASSIUM (UNII: 0BZ5A00FQU)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Verapamil Hydrochloride?
- RxCUI: 897666 - verapamil HCl 120 MG Oral Tablet
- RxCUI: 897666 - verapamil hydrochloride 120 MG Oral Tablet
- RxCUI: 897683 - verapamil HCl 80 MG Oral Tablet
- RxCUI: 897683 - verapamil hydrochloride 80 MG Oral Tablet
- RxCUI: 897722 - verapamil HCl 40 MG Oral Tablet
* 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".