NDC 53808-0329 Verapamil Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53808 - State Of Florida Doh Central Pharmacy
- 53808-0329 - Verapamil Hydrochloride
Product Characteristics
Product Packages
NDC Code 53808-0329-1
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product Details
What is NDC 53808-0329?
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:
- SODIUM ALGINATE (UNII: C269C4G2ZQ)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POVIDONE (UNII: FZ989GH94E)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- HYPROMELLOSE (UNII: 3NXW29V3WO)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
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
* 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".