NDC 40032-030 Monobasic Sodium Phosphate And Dibasic Sodium Phosphate

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
40032-030
Proprietary Name:
Monobasic Sodium Phosphate And Dibasic Sodium Phosphate
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Novel Laboratories, Inc.
Labeler Code:
40032
Start Marketing Date: [9]
01-20-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE TO OFF-WHITE)
Shape:
OVAL (C48345)
Size(s):
18 MM
Imprint(s):
N;03
Score:
2

Product Packages

NDC Code 40032-030-01

Package Description: 100 TABLET in 1 BOTTLE

Product Details

What is NDC 40032-030?

The NDC code 40032-030 is assigned by the FDA to the product Monobasic Sodium Phosphate And Dibasic Sodium Phosphate which is product labeled by Novel Laboratories, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 40032-030-01 100 tablet in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Monobasic Sodium Phosphate And Dibasic Sodium Phosphate?

Monobasic Sodium Phosphate and Dibasic Sodium Phosphate Tablets are indicated for cleansing of the colon as a preparation for colonoscopy in adults 18 years of age or older.

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:

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Product Footnotes

[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".