NDC 58354-101 Zantanol Tab.
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 58354-101?
What are the uses for Zantanol Tab.?
Which are Zantanol Tab. UNII Codes?
The UNII codes for the active ingredients in this product are:
- MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- MAGALDRATE (UNII: 6V88E24N5T)
- MAGALDRATE ANHYDROUS (UNII: 0MFM55849I) (Active Moiety)
Which are Zantanol Tab. 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:
- ALMASILATE (UNII: OZQ8O62H53)
- RANITIDINE HYDROCHLORIDE (UNII: BK76465IHM)
- LOW-SUBSTITUTED HYDROXYPROPYL CELLULOSE (8% HYDROXYPROPYL: 140000 MW) (UNII: U466TXA0AK)
- CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561)
- HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- WATER (UNII: 059QF0KO0R)
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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".