NDC 54868-5614 Sotalol Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5614 - Sotalol Hydrochloride
Product Characteristics
14 MM
E170
Product Packages
NDC Code 54868-5614-0
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 54868-5614-1
Package Description: 20 TABLET in 1 BOTTLE
Product Details
What is NDC 54868-5614?
What are the uses for Sotalol Hydrochloride?
Which are Sotalol Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- SOTALOL HYDROCHLORIDE (UNII: HEC37C70XX)
- SOTALOL (UNII: A6D97U294I) (Active Moiety)
Which are Sotalol 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)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
What is the NDC to RxNorm Crosswalk for Sotalol Hydrochloride?
- RxCUI: 1923422 - sotalol HCl 120 MG Oral Tablet
- RxCUI: 1923422 - sotalol hydrochloride 120 MG Oral Tablet
- RxCUI: 1923424 - sotalol HCl 160 MG Oral Tablet
- RxCUI: 1923424 - sotalol hydrochloride 160 MG Oral Tablet
- RxCUI: 1923426 - sotalol HCl 80 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".