NDC 0603-4170 K-effervescent
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0603 - Qualitest Pharmaceuticals
- 0603-4170 - K-effervescent
Product Characteristics
Product Packages
NDC Code 0603-4170-16
Package Description: 30 TABLET, EFFERVESCENT in 1 BOX
Price per Unit: $0.19693 per EA
Product Details
What is NDC 0603-4170?
What are the uses for K-effervescent?
Which are K-effervescent UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM BICARBONATE (UNII: HM5Z15LEBN)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
Which are K-effervescent 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:
- SORBITOL (UNII: 506T60A25R)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- SACCHARIN SODIUM ANHYDROUS (UNII: I4807BK602)
- POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
What is the NDC to RxNorm Crosswalk for K-effervescent?
- RxCUI: 1088772 - potassium bicarbonate 25 MEQ Effervescent Oral Tablet
- RxCUI: 1088772 - K+ bicarbonate 25 MEQ Effervescent Oral Tablet
- RxCUI: 1088772 - Pot bicarbonate 25 MEQ Effervescent Oral Tablet
- RxCUI: 1088772 - potassium bicarbonate 978 MG Effervescent Oral Tablet
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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".