NDC 40032-030 Monobasic Sodium Phosphate And Dibasic Sodium Phosphate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 40032 - Novel Laboratories, Inc.
- 40032-030 - Monobasic Sodium Phosphate And Dibasic Sodium Phosphate
Product Characteristics
Product Packages
NDC Code 40032-030-01
Package Description: 100 TABLET in 1 BOTTLE
Product Details
What is NDC 40032-030?
What are the uses for Monobasic Sodium Phosphate And Dibasic Sodium Phosphate?
Which are Monobasic Sodium Phosphate And Dibasic Sodium Phosphate UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- SODIUM PHOSPHATE, DIBASIC ANHYDROUS (UNII: 22ADO53M6F)
Which are Monobasic Sodium Phosphate And Dibasic Sodium Phosphate 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:
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)
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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".